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Disposable Probes for Advanced Aesthetic Technologies: Safety, Performance, and Growth

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Disposable probes for advanced aesthetic technologies are single-use applicators or tips that attach to energy-based devices such as lasers, intense pulsed light systems, radiofrequency platforms, ultrasound devices, and combination platforms. They are designed to be used for a single patient treatment session and then safely discarded to reduce infection risks, improve procedural consistency, and support regulatory compliance in modern medical aesthetics.

What Are Disposable Probes for Advanced Aesthetic Technologies?

Disposable probes for advanced aesthetic technologies are sterile, pre-packaged interfaces that connect the core device to the skin or subdermal tissue. They can take the form of microneedling cartridges, radiofrequency pins, ultrasound cartridges, laser handpiece tips, or cooling and contact modules that shape, focus, or modulate the delivered energy.

These single-use aesthetic device probes are engineered to match specific parameters of the parent system, including spot size, penetration depth, pulse duration, energy density, and cooling characteristics. In practice, they are matched to protocols for skin rejuvenation, pigmentation correction, vascular treatments, hair removal, acne management, scar revision, body contouring, tightening, and cellulite reduction.

A typical disposable probe includes a biocompatible outer shell, an energy transmission surface (such as sapphire, glass, coated metal, or insulated needles), internal mechanical or optical components, and a connector that ensures proper alignment and device recognition. Many modern systems embed RFID chips or mechanical keys in their single-use probes to prevent reuse and ensure the device automatically adjusts to the intended treatment mode.

Why Clinics Use Single-Use Aesthetic Device Probes

Modern medical aesthetic practices increasingly rely on single-use aesthetic device probes to meet rising patient expectations, rigorous safety guidelines, and insurer or regulator standards. Advanced energy-based devices generate heat, create micro-injuries, and sometimes break the epidermal barrier, all of which elevate the risk of contamination if reusable components are not perfectly disinfected every time.

Disposable probes reduce reliance on manual cleaning and high-level disinfection workflows that can be inconsistent across teams, shift schedules, and locations. They offer a standardized sterile interface for microneedling, fractional radiofrequency, ablative and non-ablative laser resurfacing, and transcutaneous drug delivery procedures. This standardization helps clinics scale treatments, train staff more efficiently, and deliver predictable outcomes, especially in high-volume medspa and dermatology settings.

Single-use probes also align with evolving infection control guidelines that increasingly favor sterile, single-patient components for procedures involving mucosa, damaged skin, or blood exposure. In many markets, clinics use single-use probes not only as a safety measure but also as a differentiator in marketing, where “sterile, disposable contact modules” and “one-time-use tips” signal quality and care.

Core Technology: How Disposable Probes Work on Advanced Platforms

Laser and IPL disposable tips

For lasers and intense pulsed light systems, disposable tips often function as optical windows, contact cooling interfaces, and spot-size definers. A sapphire or glass window transmits laser or broadband light while integrated cooling maintains epidermal protection. The geometry of the tip shapes the beam, defining fluence and spot size at the skin.

In hair removal and pigmentation devices, disposable tips maintain a pristine optical interface and consistent contact pressure, reducing hot spots and improving fluence uniformity across the treated area. Some tips are designed for small, sensitive zones such as the upper lip, periocular region, or fingers, while others are larger and optimized for back, legs, or torso treatments where speed is crucial.

Radiofrequency and RF microneedling probes

Radiofrequency disposable probes often feature multiple conductive pins or insulated microneedles arranged in arrays. In RF microneedling devices, single-use cartridges contain sterile needles that penetrate to pre-set depths while radiofrequency energy is delivered through their tips or along their shafts to create controlled coagulation in the dermis.

These probes are engineered to manage impedance, heat distribution, and penetration uniformity. By using a new probe for each patient, the system preserves needle sharpness, reduces drag and trauma, and supports sterility in procedures that intentionally break the skin barrier. Adjustable depth cartridges and different pin configurations enable customized protocols for acne scars, wrinkles, pore size, and textural irregularities.

Ultrasound and HIFU cartridges

Ultrasound and high-intensity focused ultrasound platforms use disposable cartridges that define focal depth, line length, and energy pattern. Each cartridge contains a transducer and coupling membrane designed for a specific depth, for example superficial dermis, deep dermis, or superficial muscular aponeurotic system (SMAS) for lifting and tightening.

Disposable ultrasound cartridges are often rated for a set number of lines or shots. A new cartridge provides consistent acoustic coupling and stable energy delivery, while built-in tracking mechanisms ensure the system stops output once the shot count is reached. This protects both the patient and the device by preventing the use of degraded transducers that could reduce efficacy or cause overheating.

Cryolipolysis, body contouring, and other applicators

Some body contouring and cryolipolysis systems include semi-disposable liners, membranes, or applicator inserts. While the core handpiece may be reusable, the membrane that contacts the skin and encapsulates cooling gel or vacuum interface is single-use. This approach combines durable capital equipment with disposable consumables that protect both patient and device.

Other hybrid platforms incorporate disposable tips for plasma, low-level light therapy, and non-invasive bio-stimulation, particularly when treatments involve mucosal surfaces or open tissue. Across all categories, the goal is the same: isolate the patient interface into a controlled, sterile, single-use probe.

Market Trends and Data for Disposable Aesthetic Device Probes

The market for disposable probes in advanced aesthetic technologies is closely tied to the energy-based aesthetic devices market, which has reported multibillion-dollar valuations and a strong double-digit compound annual growth rate through the mid-2030s. As more clinics adopt laser, RF, IPL, ultrasound, and combination systems, the recurring demand for consumables such as single-use probes, cartridges, and tips rises in parallel with procedure volume.

Growth in medspa chains, franchised aesthetic clinics, and branded treatment programs further reinforces the trend toward standardized disposables. These business models prioritize repeatable outcomes, consistent infection control, and predictable cost per treatment, which align with disposable probe economics. Training large numbers of providers on complex reprocessing workflows is difficult; by contrast, a clearly labeled single-use probe simplifies operations and reduces the risk of protocol deviation.

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Patient expectations also shape this market. Clients increasingly ask about sterility, cross-contamination, and the use of new or sealed components, especially in post-pandemic environments where infection awareness is heightened. Disposable probes, single-use gel packets, and sterile tip packaging become visible assurance elements during consultation and treatment.

From the manufacturer perspective, integrating consumables into device ecosystems creates recurring revenue streams that support research and development, post-market surveillance, and training programs. As a result, many manufacturers now design platforms from the ground up with proprietary disposable tips and cartridges that are essential to the device’s core function.

Types of Disposable Probes in Advanced Aesthetic Systems

Disposable probes for advanced aesthetic technologies can be grouped into several functional categories, each tailored to specific procedures and treatment objectives.

Common types include:

  • Microneedling RF cartridges with insulated or non-insulated pins.

  • Fractional laser treatment tips for ablative and non-ablative resurfacing.

  • IPL and laser contact cooling windows and spot-size adapters.

  • HIFU and ultrasound lifting cartridges with different focal depths.

  • Cryolipolysis membranes and liners.

  • Plasma, RF, or hybrid applicator tips for delicate areas.

  • Endoluminal or intravaginal probes designed for mucosal tissue treatments.

Within each category, manufacturers differentiate based on tip geometry, depth increments, energy profile, flexibility, surface coating, and the integration of sensors or recognition chips. For example, RF microneedling cartridges may provide 10, 25, or 49 pins with adjustable depths ranging from very superficial to several millimeters, while HIFU cartridges may be dedicated to 1.5 mm, 3.0 mm, or 4.5 mm focal depths with specific shot counts.

Clinics often stock multiple probe types for each platform to support individualized plans. For a single patient, a provider might use one cartridge for deep tightening and another for superficial smoothing, swapping probes mid-session to layer different depths and energy densities in a controlled way.

Benefits of Disposable Probes for Clinics and Patients

Disposable probes for advanced aesthetic technologies deliver value on several levels: safety, clinical performance, workflow efficiency, and business outcomes.

On the safety side, single-use probes minimize cross-contamination and reduce dependence on complex reprocessing steps that require strict adherence to manufacturer instructions, enzymatic cleaners, specific disinfection agents, and documented dwell times. For treatments that involve bleeding, exudate, or mucosal contact, disposable probes align with best practice recommendations that favor sterile, single-use interfaces.

From a performance perspective, using a fresh probe for every patient ensures sharp microneedles, intact coatings, consistent transmission surfaces, and clean windows free of micro-scratches or residue. This consistency supports more uniform energy delivery, predictable thermal profiles, and more repeatable clinical outcomes across sessions and providers.

Workflow-wise, disposable probes save time between patients by eliminating the need to soak, scrub, rinse, dry, inspect, and track reusable parts. Staff can simply dispose of the used probe in an appropriate container, mount a new one, confirm device recognition, and proceed. This is particularly valuable in high-throughput clinics where room turnover time directly affects revenue.

Financially, disposable probe models allow clinics to map per-treatment consumable costs and integrate them into pricing, making margins easier to calculate and forecast. Although the cost of single-use probes adds to each session, reduced staff time for reprocessing, fewer device downtime events due to damage, and lower infection-related risk often offset that expense.

Clinical Safety, Compliance, and Infection Control

Disposable probes play a crucial role in modern infection control strategies for dermatology, plastic surgery, and medical aesthetics. Clinical guidelines increasingly emphasize the use of sterile, single-use components for procedures where the skin barrier is compromised or where probes contact mucous membranes or contaminated sites.

In microneedling RF treatments, fractional ablative laser resurfacing, and invasive tightening procedures, using a fresh, sterile probe for each patient is a straightforward way to minimize the risk of transmitting pathogens. Single-use tips eliminate the variability that arises when different staff members perform manual cleaning on complex, small-diameter channels and internal surfaces.

For ultrasound and HIFU, probe covers and coupling media are important, but there is growing recognition that sterile, one-time-use interfaces offer an additional layer of safety. When matched with appropriate disinfection practices for the reusable body of the device, disposable cartridges complete a comprehensive infection control protocol.

Regulatory bodies and professional societies also pay close attention to documentation. Many single-use probes include traceable lot numbers and indicators on packaging so clinics can log which batch was used on which patient. This enhances overall quality management systems, supports audits, and enables rapid response in the unlikely event of a field safety notice or recall.

Economic Impact and ROI of Single-Use Aesthetic Probes

At first glance, clinics may perceive disposable probes as a cost driver because they add a recurring expense to each treatment. However, a more complete return-on-investment analysis often reveals that single-use aesthetic device probes can improve long-term profitability.

Key economic considerations include:

  • Reduction in staff time dedicated to cleaning, disinfection, drying, and storage of reusable probes.

  • Lower risk of device damage from harsh chemicals, improper soaking, or mechanical abrasion during cleaning.

  • Fewer cancellations or complications related to questionable probe sterility or delayed reprocessing cycles.

  • Enhanced ability to price treatments confidently with clear consumable costs.

  • Potential premium pricing for “sterile disposable-tip” protocols and patient-perceived value.

When clinics calculate the total cost of ownership for advanced aesthetic technologies, including energy-based platforms, disposables should be factored in alongside maintenance, training, and marketing. Many providers find that the predictability, safety, and branding advantages of disposable probes justify their incremental cost, especially in competitive urban markets where patient expectations and online reviews shape demand.

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Company Background: ALLWILL’s Role in the Disposable Probe Ecosystem

ALLWILL is redefining B2B medical aesthetics by focusing on innovation, trust, and efficiency, delivering not only devices but also integrated solutions that address sourcing, maintenance, and upgrade challenges for busy practitioners. Through its Smart Center for device inspection, repair, and refurbishment, along with the MET vendor management system and Lasermatch inventory platform, ALLWILL helps clinics access high-performance energy-based devices and compatible consumables, including single-use probes, with transparency and data-driven decision support.

Buying Guide: How to Select Disposable Probes for Advanced Aesthetic Technologies

Choosing the right disposable probes for advanced aesthetic technologies requires careful evaluation of device compatibility, clinical objectives, regulatory environment, and practice workflow. For each platform, clinics should start by reviewing the manufacturer’s approved probe catalog and confirming that each tip or cartridge is specifically designed and validated for that device model.

Important factors include:

  • Energy modality and indication: Determine whether you need probes for hair removal, skin resurfacing, scar revision, pigmentation, vascular lesions, tightening, contouring, or intimate health, and confirm that each probe is indicated for the desired application.

  • Depth and geometry: For RF microneedling and HIFU, align probe depth and pattern with the anatomical targets, such as superficial dermis, deep dermis, or SMAS.

  • Skin type compatibility: Verify that the probe and protocol are suitable for the Fitzpatrick skin types in your patient population, especially for devices that deliver heat or light.

  • Sterilization method and packaging: Ensure that all single-use probes are supplied sterile, labeled clearly, and packaged to maintain integrity until point of use.

  • Traceability and documentation: Look for lot numbers, expiry dates, and labeling that support your clinic’s documentation and quality management requirements.

Training and support are also paramount. Providers should receive clear instructions for mounting, priming, and removing disposable probes, as well as information on recognizing damaged or compromised packaging. Many clinics integrate disposable probe checks into pre-treatment time-outs and safety checklists.

Top Categories of Disposable Probes and Their Use Cases

The disposable probe landscape spans several key product categories that map directly to high-demand aesthetic procedures.

A few of the most widely used categories include:

  • RF microneedling cartridges for texture, scars, fine lines, and stretch marks on the face, neck, and body.

  • Fractional laser tips for ablative and non-ablative resurfacing of wrinkles, dyschromia, and photoaging.

  • HIFU cartridges for non-surgical lifting of the lower face, neck, and brow.

  • IPL and laser tips for hair removal, vascular lesions, and pigment correction on diverse body areas.

  • Cryolipolysis membranes for localized fat reduction on abdomen, flanks, thighs, and arms.

  • Specialized gynecological or intimate health probes designed for mucosal tissue and pelvic floor support.

In many device ecosystems, these probes are offered in tiered lines that align with different practice models. Entry-level probes may target general indications at standard speeds, while premium lines emphasize faster coverage, enhanced comfort, or advanced cooling for sensitive or high-risk areas.

Competitor Comparison: Key Dimensions in Disposable Probe Solutions

When evaluating disposable probes across different device manufacturers and brands, clinics should compare multiple dimensions beyond simple per-unit cost. Core differentiators often include energy delivery precision, patient comfort, integration with device software, availability of protocols, and support.

Example dimensions that clinics frequently evaluate:

  • Range of available probe types and depths for a given platform.

  • Level of automation in probe recognition and parameter locking.

  • Ergonomics and feedback for the provider, including grip, weight, and visual alignment markers.

  • Built-in safety features such as temperature monitoring or impedance tracking.

  • Environmental footprint, including packaging size, materials, and potential recyclability programs.

Some vendors also differentiate with training programs that teach evidence-based protocols for each probe type, including photography standards, dosing strategies, and post-care guidelines. For multi-site organizations, the ability to standardize on a consistent probe portfolio across locations can simplify inventory management, protocol rollout, and quality control.

Real User Cases: ROI and Clinical Outcomes from Disposable Probes

Consider a medspa that migrated from reusable microneedling tips to RF microneedling cartridges with disposable probes. Before the transition, the clinic required 20 to 30 minutes of staff time per patient to soak, scrub, disinfect, and document reusable tips, with occasional scheduling delays when insufficient probes were available. After adopting single-use RF cartridges, turnover time dropped, more appointments were opened per day, and staff redeployed time to consultation and follow-up.

Another example is a dermatology group that upgraded its vascular and pigment treatment suite with laser and IPL systems configured for single-use cooling tips. These tips helped standardize contact pressure and improve tolerance in patients with sensitive skin, which in turn reduced the need for topical anesthetics and their associated preparation time. The clinic reported higher patient satisfaction scores and more predictable treatment courses across providers.

In a plastic surgery practice, HIFU cartridges with defined shot counts and disposable coupling interfaces helped reduce variability in lifting results. By tracking cartridge usage per patient and per area, surgeons fine-tuned their protocols and pricing, aligning expectations and outcomes while maintaining precise cost control.

Regulatory and Environmental Considerations

Disposable probes for advanced aesthetic technologies sit at the intersection of medical device regulation, infection control guidance, and environmental sustainability. On the regulatory side, single-use probes must comply with medical device standards for biocompatibility, sterilization validation, packaging integrity, and labeling.

Infection control and occupational safety frameworks encourage or require single-use patient interfaces for specific procedures and risk levels, particularly where bloodborne pathogens or high-risk infectious agents are a concern. Clinics adopting disposable probes must still follow appropriate sharps and biohazard waste protocols, even though probes reduce the volume of chemical disinfectants used on-site.

Environmental impact remains an active discussion area. Single-use probes generate waste, and clinics need clear pathways for segregation, safe disposal, and, where available, specialized recycling programs for certain plastics or metals. Some manufacturers are exploring reduced packaging, recyclable materials, and take-back programs that recover embedded metals or electronics from used probes.

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Balancing patient safety with environmental responsibility requires a clinic-wide strategy that includes supplier selection, waste segregation training, and participation in sustainability initiatives without compromising infection control.

Integration with Practice Management and Inventory Systems

As single-use probes become central to advanced aesthetic workflows, efficient inventory management gains importance. Clinics must maintain adequate stock levels across multiple probe types, depths, and indications to avoid treatment delays and suboptimal substitutions.

Integrating probe ordering with practice management or inventory platforms can automate reordering thresholds, track usage patterns, and forecast demand based on scheduled appointments. Multisite practices benefit from centralized visibility into consumable usage across locations, enabling optimized purchasing and better negotiation with suppliers.

When disposable probes are tied to device software through recognition chips or serialized codes, usage data can also inform maintenance schedules, uptime metrics, and clinical performance analytics. For example, a clinic could correlate the number of probes used per device with revenue per room, treatment outcomes, or training needs.

Training, Protocols, and Patient Education

Safe and effective use of disposable probes for advanced aesthetic technologies depends on thorough provider training. Clinicians and technicians need to understand how each probe type modifies energy distribution, penetration depth, and thermal effects, as well as how to adjust parameters based on skin type, age, and concern.

Training should cover:

  • Proper storage and handling of sterile packaged probes.

  • Visual inspection of packaging and probe integrity before use.

  • Correct mounting, priming, and dismounting sequences.

  • Recognition of device alerts related to probe compatibility or shot count limits.

  • Documentation of lot numbers and probe types in patient records.

Patient education is equally important. During consultation, providers can explain the role of single-use probes in infection control and treatment precision, addressing concerns about safety and value. Highlighting that each patient receives their own new, sterile tip or cartridge can build trust and support treatment acceptance.

Future Trends: Smart Probes, Personalization, and Data

The next generation of disposable probes for advanced aesthetic technologies is likely to incorporate more sensor integration, data connectivity, and personalization features. Smart probes may include temperature sensors, impedance monitors, motion tracking, or microcameras that feed real-time information back to the device and operator.

These capabilities can enable dynamic energy modulation that adjusts pulse duration, cooling intensity, or shot density based on the patient’s tissue response in real time. Over multiple sessions, accumulated data from disposable probes could help refine clinic protocols, segment patients into response profiles, and support more personalized treatment plans.

Another emerging trend is modular probe design, where a base component houses electronics or sensors and a smaller, less expensive sterile insert provides the skin-contacting interface. This hybrid approach aims to balance safety, performance, and environmental impact.

As the energy-based aesthetic devices market continues to expand and diversify, disposable probes will remain essential to delivering safe, high-quality, and scalable treatments. Clinics that understand how to select, use, and manage these single-use components strategically will be better positioned to serve patients, control risk, and capture long-term growth in advanced medical aesthetics.

FAQ

Q: What are Disposable Probes for Advanced Aesthetic Technologies and why matter for safety and performance?
A: Disposable Probes reduce cross-contamination, ensure consistent energy delivery, and simplify maintenance, boosting patient safety and device performance while lowering downtime and service costs for clinics. ALLWILL supports practitioners with vetted consumables and reliable sourcing.

Q: How does safety improve when using single-use probes in aesthetic tech?
A: Single-use probes eliminate residue buildup and wear that can affect accuracy, delivering reliable results and reducing infection risk, which translates to higher treatment confidence and practitioner trust.

Q: Which performance benefits come from using disposable probes in advanced devices?
A: Probes provide consistent impedance and laser/treatment output, improving repeatability across sessions and practitioners, which leads to predictable results and better client satisfaction.

Q: What should buyers consider when selecting disposable probes?
A: Look for compatibility with your device model, sterile packaging, certified biocompatibility, supply stability, and cost-per-use to balance quality with budget.

Q: How do disposable probes support growth in aesthetic practices?
A: Reliable consumables minimize downtime, enable faster treatment cycles, and reduce warranty issues, helping clinics expand throughput and attract more clients.

Q: Are there regulatory or compliance points to watch for?
A: Confirm traceability, batch-level QA documentation, and vendor certifications, ensuring you meet local health and safety standards.

Q: What role does ALLWILL play in disposable probe procurement?
A: ALLWILL provides brand-agnostic sourcing, refurbishment options, and a transparent supply chain that aligns with safety, performance, and cost goals for practices.

Q: How can I assess total cost when adopting disposable probes?
A: Compare upfront price, per-treatment cost, waste handling, and downtime impact; choose suppliers offering predictable budgeting and reliable replenishment.

Conversion-Focused Next Steps for Clinics

Clinics evaluating disposable probes for advanced aesthetic technologies can start by auditing their current treatment mix, procedure volume, and infection control protocols to identify where single-use probes would provide safety and workflow advantages. Next, they can consult with device manufacturers, solution partners, and trusted advisors to align platform selection, probe portfolios, and training plans with their strategic goals.

Finally, integrating disposable probe costs and value into pricing, patient communication, and marketing helps ensure that these technologies support both high-quality outcomes and sustainable profitability. By treating single-use aesthetic device probes as core strategic assets rather than incidental consumables, modern practices can elevate their standard of care and stand out in an increasingly competitive aesthetic landscape.

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(b) Special Order Product. If this Agreement includes the sale of a product that MRP does not currently have or typically keep in stock, in MRP’s sole determination, but is acquired from a third party specifically for Buyer (a “Special Order Product”), then Buyer agrees that (i) Buyer, at its sole discretion, has made the selection of such Special Order Product, (ii) such Special Order Product is being acquired by MRP solely at the request of Buyer, (iii) no representation, warranty or guarantee has been made by MRP with respect to such Special Order Product, (iv) the obligation of Buyer to pay MRP for the Special Order Product is absolute and unconditional, and (v) Buyer waives and releases MRP from all claims, damages and losses arising out of such Special Order Product. Special Order Products carry no right to inspection before or after delivery, and MRP is not responsible for examining or evaluating such Special Order Products. MRP makes no warranty about Special Order Products and offerings of the third party (including description of the Special Order Product). MRP does not assume any responsibility or liability for the actions, product and content of all these and any other third parties. If there are any problems with any Special Order Product, Buyer must contact the manufacturer of such Special Order Product for assistance.

(c) Limited Warranties, If Any.

(i) If the Quote expressly states that the Equipment has a warranty for a certain time (a “Warranty Period”), then MRP warrants that the Equipment shall be in good working order under normal use for the Warranty Period, which Warranty Period shall commence from the date of delivery to Buyer (the “Delivery Date”), unless otherwise approved by an MRP Officer in writing, except for the following: (A) New (not used or pre-owned) Equipment that is to be serviced by MRP: if the Quote is silent, warranted to be in good working order under normal use for one hundred eighty (180) days from the Delivery Date; (B) Used Equipment sold refurbished by MRP: if the Quote is silent, warranted to be in good working order under normal use for thirty (30) days from the Delivery Date; (C) Consumable/disposable Equipment: if the Quote is silent, warranted to have been shipped from MRP in functional condition, and no additional warranty shall apply; no service shall be provided either. These items should be inspected for obvious damage, subject to Section 6 and 8(e), and MRP’s obligation under this warranty and this Section 8(c)(i)(C) is limited to replacement of the Equipment; and (D) New (not used or pre-owned) Equipment that is to be serviced by the manufacturer: if the Quote is silent, MRP makes no warranty for any such Equipment. Buyer’s sole warranty for any such Equipment, if any, shall be the original manufacturer’s warranty, which MRP agrees to pass on to Buyer, as applicable. (ii) For the limited warranties of Section 8(c)(i), including exceptions (A) and (B), but not (C) or this (D), Buyer is entitled to telephone, e-mail and video technical assistance and, subject to Sections 8(d) and 8(e), repair or replacement of such Equipment, in MRP’s sole discretion, should the Equipment become inoperative through normal use during the Warranty Period. Loaner equipment is not provided, but if so arranged by MRP, Buyer shall pay MRP the cash list price of any unreturned loaner equipment provided by MRP within seven (7) days of a written demand from MRP. (iii) Repair or replacement under any limited warranty of Equipment may be with parts or products that are new, used or refurbished, carrying the same limited warranty for the remaining term of the original item. Repairs or replacements shall not interrupt, extend or prolong the term of the warranty. (iv) For Services purchased under this Agreement, MRP warrants that the Services shall be performed using competent personnel in a professional manner in accordance with generally recognized industry standards for similar services. Subject to Sections 6 and 8(e) herein, if any Service was not performed in accordance with the aforementioned warranty, then MRP shall, in its sole discretion, either (A) repair or re-perform the applicable Service, or (B) credit or refund the price of such Service at the pro rata contract rate.

(d) Exclusions. MRP reserves the right, without liability, to void all warranties and remedies, including any obligation to service, repair, replace or otherwise remedy defects, errors or failures of the Equipment due to the occurrence of any of these events, and MRP shall be in no way responsible for: (i) handling, maintenance or use in a manner that is inconsistent with and/or contrary to the original manufacturer’s or MRP’s recommended procedures and/or instructions, including, without limitation, use of or with an unauthorized third-party good or part; (ii) any failure or damage resulting from negligence, alteration, modification or relocation of the Equipment by Buyer, its employees, agents or representatives; (iii) attempted or actual unauthorized dismantling, disassembling, service, repair, addition or change of the Equipment, including, without limitation, changing the serial number or shot count; (iv) abnormal wear and tear, including, without limitation, use under abnormal conditions (e.g., unclean, dusty, or exposure to extreme electromagnetic radiation, temperature or humidity); or (v) damage or failure of the Equipment due to a Force Majeure Event or a problem in the premises of the Equipment. In any of the above situations, or for any Equipment that has no warranty, MRP has sole discretion to service the Equipment, at Buyer’s expense, at MRP’s then-in-effect rates for service, labor, travel, shipping and materials.

(e) Notice and Inspection. The limited warranties contained in this Section 8 are made on condition that immediate written notice of any noncompliance with the Equipment’s and/or the Service’s warranty be given to MRP, and provided that MRP’s inspection reveals that Buyer’s claim is valid under the terms of such warranty.

        9.  DISCLAIMERS; NO OTHER WARRANTY. EXCEPT TO THE EXTENT AS PROVIDED IN SECTION 8(c)(i)(D), BUYER ACKNOWLEDGES THAT MRP IS NOT BOUND BY ANY WARRANTY THAT MAY BE SET FORTH IN A MANUFACTURER’S WRITTEN MATERIALS THAT WOULD HAVE APPLIED HAD BUYER PURCHASED THE EQUIPMENT DIRECTLY FROM THE MANUFACTURER IN ITS UNUSED STATE. BUYER ACKNOWLEDGES THAT BUYER HAS NOT RELIED UPON ANY WARRANTY OTHER THAN AS SET FORTH IN THIS AGREEMENT. IN ADDITION, BUYER ALSO HEREBY ACKNOWLEDGES AND AGREES THAT ANY ORAL OR WRITTEN STATEMENTS CONCERNING USE AND REGULATION OF MEDICAL DEVICES SOLD BY MRP ARE AND SHALL BE CONSTRUED AS FOR INFORMATIONAL PURPOSES ONLY AND WITHOUT WARRANTY OR ASSURANCE BY MRP AS TO THEIR ACCURACY OR VALIDITY. MRP ALSO HEREBY DISCLAIMS ANY AND ALL WARRANTIES REGARDING OTHER MEDICAL CARE OR HELP, INCLUDING THE SELECTION OF AESTHETIC AND MEDICAL PROCEDURES AND PRODUCTS FOR, OR CARE OF, PATIENTS. THE LIMITED WARRANTIES OF THIS AGREEMENT, IF APPLICABLE TO ANY EQUIPMENT OR SERVICE FURNISHED UNDER THIS AGREEMENT, CONSTITUTE THE ONLY WARRANTIES MADE WITH RESPECT TO THE EQUIPMENT AND/OR SERVICE AND ANY DEFECT, DEFICIENCY OR NONCONFORMITY. TO THE EXTENT PERMITTED BY LAW, SUCH WARRANTY IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESS OR IMPLIED BY LAW, COURSE OF DEALING, COURSE OF PERFORMANCE, USAGE OF TRADE OR OTHERWISE, INCLUDING, BUT NOT LIMITED TO, ANY EXPRESS OR IMPLIED WARRANTY OF MERCHANTABILITY, TITLE, NONINFRINGEMENT OR FITNESS FOR A PARTICULAR PURPOSE.

        10.  LIMITATION OF LIABILITY. NOTWITHSTANDING ANYTHING TO THE CONTRARY IN THIS AGREEMENT, UNDER NO CIRCUMSTANCES SHALL MRP BE LIABLE FOR ANY INDIRECT, PUNITIVE, INCIDENTAL, CONSEQUENTIAL, EXEMPLARY OR SPECIAL DAMAGES, ARISING FROM, RELATED TO OR CAUSED, DIRECTLY OR INDIRECTLY, WHETHER FORESEEABLE OR NOT, BY THE EQUIPMENT AND/OR THE SERVICES, THE USE OR INABILITY TO USE THE EQUIPMENT, THE RESULTS GENERATED FROM THE EQUIPMENT AND/OR THE SERVICES, THIS AGREEMENT, ANY OTHER ACT OR OMISSION OF MRP, OR BASED UPON ANY OTHER LEGAL THEORY. IN NO EVENT SHALL MRP BE LIABLE FOR ANY LOSSES OF REVENUE, USE, BUSINESS OPPORTUNITY, PROFIT, SAVINGS OR ANY OTHER DAMAGES DUE TO ANY CAUSE WHATSOEVER, EVEN IF MRP OR ITS AGENTS HAS BEEN ADVISED OF THE POSSIBILITY THEREOF. THE FOREGOING IS A SEPARATE, ESSENTIAL TERM OF THIS AGREEMENT, AND SHALL BE EFFECTIVE UPON THE FAILURE OF ANY REMEDY, EXCLUSIVE OR NOT. IN NO EVENT WILL MRP’S TOTAL LIABILITY UNDER THIS AGREEMENT EXCEED THE PURCHASE PRICE ACTUALLY PAID TO MRP BY BUYER FOR THE EQUIPMENT AND/OR THE SERVICES GIVING RISE TO THE CLAIM FOR WHICH DAMAGES ARE BEING SOUGHT. NO SUIT OR ACTION MAY BE BROUGHT BY BUYER, ITS SHAREHOLDERS, DIRECTORS, MANAGERS, EMPLOYEES OR AGENTS FOR ANY BREACH OF THIS AGREEMENT MORE THAN ONE (1) YEAR AFTER THE ACCRUAL OF SUCH CAUSE OF ACTION. IT IS AGREED THAT MRP’S LIABILITY IS SO LIMITED. WITHOUT LIMITING THE GENERALITY OF THE FOREGOING, BUYER ASSUMES ALL RISK AND LIABILITY FOR THE RESULTS OBTAINED BY THE USE OF ANY EQUIPMENT IN THE PRACTICE OF ANY PROCESS, WHETHER IN TERMS OF OPERATING COSTS, GENERAL EFFECTIVENESS, SUCCESS OR FAILURE, AND REGARDLESS OF ANY ORAL OR WRITTEN STATEMENTS MADE BY MRP, BY WAY OF TECHNICAL ADVICE OR OTHERWISE, RELATED TO THE USE OF THE EQUIPMENT.

        11.  BUYER’S REPRESENTATIONS AND WARRANTIES. Buyer represents and warrants to MRP that: (a) Buyer is duly organized, validly existing, and in good standing in the jurisdiction of Buyer’s formation; (b) Buyer is duly qualified to do business and is in good standing in every jurisdiction in which such qualification is required; (c) Buyer has the full right, power, and authority to enter into this Agreement and to perform Buyer’s obligations under this Agreement; (d) the execution of this Agreement by the person whose signature is set forth at the end hereof has been duly authorized by all necessary corporate action of Buyer; (e) when executed and delivered by each of MRP and Buyer, this Agreement will constitute the legal, valid and binding obligation of Buyer, enforceable against Buyer in accordance with its terms; (f) Buyer is in compliance with all applicable laws relating to this Agreement, the Equipment and the operation of Buyer’s business; (g) Buyer is not insolvent and is paying all of its debts as they become due; and (h) all financial information that Buyer has provided to MRP is true and accurate and fairly represents Buyer’s financial condition.

        12. PROPRIETARY RIGHTS.

(a) Ownership. No sale shall be construed as granting to Buyer any license or other right in, or to, any of MRP’s (i) patents; (ii) trademarks; (iii) internet domain names, whether or not trademarks, registered by any authorized private registrar or governmental authority, web addresses, web pages, websites and URLs; (iv) works of authorship, expressions, designs and design registrations, whether or not copyrightable, including copyrights and copyrightable works, software and firmware, technical data, data files, and databases and other specifications and documentation; (v) trade secrets; (vi) environmental or other testing applicable to the Equipment and/or the Services; and (vii) industrial and other intellectual property rights, and all rights, interests, and protections that are associated with, equivalent or similar to, or required for the exercise of, any of the foregoing, however arising, in each case whether registered or unregistered and including all registrations and applications for, and renewals or extensions of, such rights or forms of protection pursuant to the laws of any jurisdiction throughout in any part of the world (collectively, the “Intellectual Property Rights”).

(b) Prohibited Acts. Buyer shall not (i) take any action that might interfere with any of MRP’s rights in or to Intellectual Property Rights, including MRP’s ownership or exercise thereof; (ii) challenge any right, title, or interest of MRP in or to the Intellectual Property Rights; (iii) make any claim or take any action adverse to MRP’s ownership of the Intellectual Property Rights; (iv) register or apply for registrations, anywhere in the world, for MRP’s trademarks or any other trademark that is similar to MRP’s trademarks or that incorporates MRP’s trademarks in whole or in confusingly similar part; (v) use any mark, anywhere that is confusingly

similar to MRP’s trademarks in whole or in confusingly similar part; (vi) engage in any action that tends to disparage, dilute the value of or reflect negatively on the Equipment and/or the Services or any of MRP’s trademarks; (vii) misappropriate any of MRP’s trademarks for use as a domain name without prior written consent from MRP; or (viii) alter, obscure or remove any of MRP’s trademarks, or trademark or copyright notices or any other proprietary rights notices placed on the

Equipment, marketing materials or other materials that MRP may provide.

        13.  CONFIDENTIAL INFORMATION. Without the prior written consent of MRP,Buyer, directly or indirectly, shall not disclose (and will direct its directors, shareholders, employees and agents not to disclose) any Confidential Information. The term “Confidential Information” means any information of or relating to MRP or the Equipment and/or the Services not generally known to the public (other than as a result of disclosure in violation of this Agreement) in spoken, printed, electronic or any other form or medium, including, but not limited to, business processes, practices, methods, policies, plans, publications, documents, research, operations, services, strategies, techniques, agreements, contracts, transactions, potential transactions, know-how, trade secrets, databases, manuals, records, supplier information, financial information, accounting information, legal information, marketing information, pricing information, payroll information, personnel information, and supplier lists.

        14.  NON-SOLICITATION. Buyer agrees not to solicit or hire any personnel of MRP involved with the delivery of the Services during the provision of such Services and for twelve (12) months after the completion of such Services; provided, however, that Buyer may hire individuals employed by MRP who, without other solicitation, respond to advertisements or solicitations aimed at the general public.

        15.  EQUITABLE REMEDIES. Buyer acknowledges and agrees that (a) a breach or threatened breach by Buyer of any of its obligations under Sections 13 or 14 would give rise to irreparable harm to MRP for which monetary damages would not be an adequate remedy and (b) in the event of a breach or a threatened breach by Buyer of any such obligations, MRP shall, in addition to any and all other rights and remedies that may be available to MRP at law, at equity, or otherwise in respect of such breach, be entitled to equitable relief, including a temporary restraining order, an injunction, specific performance, and any other relief that may be available from a court of competent jurisdiction, without any requirement to post a bond or other security, and without any requirement to prove actual damages or that monetary damages will not afford an adequate remedy. Buyer agrees that Buyer will not oppose or otherwise challenge the appropriateness of equitable relief or the entry by a court of competent jurisdiction of an order granting equitable relief, in either case, consistent with the terms of this Section 15.

        16.  INDEMNIFICATION. Buyer agrees to indemnify, defend and hold harmless MRP and its directors, shareholders, employees and agents (collectively, “MRP Indemnitees”) against any liability, damage, loss or expense incurred by or imposed in connection with any claims, suits, actions, demands or judgments arising out of (a) any breach or non-fulfillment of any representation, warranty or covenant set forth in this Agreement by Buyer or its directors, managers, employees or agents (collectively, “Buyer’s Agents”); (b) any negligent act or omission or willful misconduct of Buyer or Buyer’s Agents in connection with this Agreement; (c) any bodily injury, death of any person or damage to real or tangible personal property caused by Buyer or Buyer’s Agents, including the use of unauthorized parts in or service of the Equipment; (d) any failure by Buyer or Buyer’s Agents to comply with any applicable laws; (e) any fraud or other intentional acts by Buyer or Buyer’s Agents; and (f) the use or operation of the Equipment, including, without limitation, any medical and/or surgical procedures performed by Buyer, and any of Buyer’s Agents, using the Equipment unless said damages are determined by a court of competence jurisdiction to be solely by the gross negligence of MRP or solely as result of a breach by MRP of the limited warranties contained herein.

        17.  DEFAULTS; REMEDIES. Notwithstanding anything herein to the contrary, should Buyer fail to pay for the order or any other amount, in whole or in part, when due or perform its other obligations under this Agreement or as otherwise mutually agreed in writing between Buyer and MRP (each, a “Default”), then MRP may take any and all actions available under law or equity to collect said amounts with a ten (10) day prior written notice, including, but not limited to, enforcing its security interest, accelerating the payment of and declaring immediately due and payable any unpaid balance of the order, referral to outside collection agencies and/or commencement of legal action. MRP’s rights shall be cumulative, and it shall not be required to have attempted to realize upon to the Equipment before taking any other collection actions. MRP may require that Buyer assemble and return any or all of the Equipment to MRP and, in the event Buyer fails to return such Equipment peaceably, enter upon the premises where such Equipment is located, with or without legal process, and repossess such Equipment. Upon a Default, Buyer agrees to pay upon MRP’s demand: (i) all costs and expenses incurred by MRP or its assignee in connection with the enforcement of any remedies, including all expenses incurred in connection with the return, sale, release or other disposition of the Equipment, including attorneys’ fees and other costs incurred by MRP or its assignee in enforcing or defending its rights and remedies under this Agreement and any other written agreement between Buyer and MRP.

        18.  COMPLIANCE WITH LAWS. Buyer shall (a) carry out the transactions contemplated by this sale and deal with the Equipment in conformity with all applicable laws, rules and regulations of all government authorities, including, without limitation, export laws, (b) obtain all permits and licenses required in connection with the purchase, shipment, installation or use of the Equipment, and (c) be solely responsible to fully understand and comply with laws, rules and regulations. Any information provided is as a convenience only.

        19.  FURTHER ASSURANCES. Upon MRP’s reasonable request, Buyer shall, at its sole cost and expense, execute and deliver all such further documents and instruments, and take all such further acts, necessary to give full effect to this Agreement.

        20.  ASSIGNMENT; SUCCESSORS AND ASSIGNS. Buyer cannot delegate any duties nor assign any rights or claims under this Agreement without MRP’s prior written consent, and any such attempt or assignment shall be void. In the event that Buyer finances its acquisition of any Equipment with a third party, Buyer may direct MRP to transfer title of such Equipment to such third-party financing company, with all remaining terms and conditions of this Agreement remaining in full force and effect. This Agreement is binding on and inures to the benefit of the parties to this Agreement and their respective permitted successors and permitted assigns.

        21.  NO THIRD-PARTY BENEFICIARIES. Subject to Section 16, this Agreement benefits solely the parties to this Agreement and their respective permitted successors and assigns, and nothing in this Agreement, express or implied, confers on any other person any legal or equitable right, benefit, or remedy of any nature whatsoever under or by reason of this Agreement.

        22.  GOVERNING LAW; VENUE. The application of the UN Convention on Contracts for the International Sale of Goods is expressly excluded. The parties agree that any and all claims, demands, disagreements, controversies or disputes arising out of or relating to this Agreement and any agreement or document delivered in connection herewith (collectively, “Claims”) shall be governed by and construed in accordance with the laws of the State of Utah and adjudicated exclusively in the state and federal courts located in or nearest to Summit County, Utah, which courts shall have the sole and exclusive jurisdiction and venue for adjudication of all Claims. The parties hereby agree upon, consent and stipulate to the jurisdiction and venue of the aforementioned courts for the adjudication of all Claims, to the exclusion of all other courts, forums and venues whatsoever.

        23.  NON-DISPARAGEMENT. Buyer shall not disparage MRP or MRP’s trademarks, websites, products or services, or display any such items in a derogatory or negative manner on any website or in any public forum or press release.

        24.  NOTICES. Any notice, demand, or communication required, permitted or desired to be given hereunder shall be deemed effectively given when personally delivered, when sent by electronic means, when received by overnight courier, or when mailed by prepaid, certified or registered mail, return receipt requested, addressed to the other party at its address set forth on the Quote or to such other address that the receiving party may designate from time to time in accordance with this Section 25.

        25.  PUBLIC ANNOUNCEMENTS. Unless otherwise stated herein, neither party shall issue a press release or otherwise advertise, make a public statement or disclose to any third-party information pertaining to the relationship arising under this Agreement, the existence or terms of this Agreement, the underlying transactions between MRP and Buyer or agent for Buyer or refer to the other party in relation to this Agreement without the other party’s prior written approval.

        26.  ENTIRE AGREEMENT; ADDITIONAL OR INCONSISTENT TERMS. Subject to Section 32, this Agreement constitutes the sole and entire agreement between the parties hereto relating to the subject matter hereof, and any unincorporated representation, affirmation of fact, course of prior dealings, promise or condition in connection therewith, or usage of the trade, shall not be binding on either party. Terms and conditions set forth which differ from, conflict with or are not included in this Agreement shall not be part of any agreement between MRP and Buyer unless both parties specifically accept such terms and conditions in writing.

        27.  WAIVER. No waiver under this Agreement is effective unless it is in writing and signed by the party waiving its right. Any waiver authorized on one occasion is effective only in that instance and only for the purpose stated and does not operate as a waiver on any future occasion. None of the following constitutes a waiver or estoppel of any right, remedy, power, privilege or condition arising from this Agreement: any failure or delay in exercising any right, remedy, power or privilege or in enforcing any condition under this Agreement; or any act, omission or course of dealing between the parties.

        28.  SURVIVAL. Subject to the limitations and other provisions of this Agreement, the representations and warranties of Buyer contained herein shall survive the expiration or earlier termination of this Agreement for a period of twelve (12) months after such expiration o termination and (b) this Section 29 and Sections 10, 12, 13, 14, 15, 16, 17, 21, 22, 23, 24, 26, and 32 of this Agreement, as well as any other provision that, in order to give proper effect to its intent, should survive such expiration or termination, shall survive the expiration or earlier termination of this Agreement. All other provisions of this Agreement shall not survive the expiration or earlier termination of this Agreement.

        29.  RELATIONSHIP OF PARTIES. Nothing in this Agreement creates any agency, joint venture, partnership or other form of joint enterprise, employment or fiduciary relationship between the parties. Neither party has any express or implied right or authority to assume or create any obligations on behalf of or in the name of the other party or to bind the other party to any contract, agreement or undertaking with any third party.

        30.  HEADINGS. The headings in this Agreement are for reference only and do not affect the interpretation of this Agreement.

        31.  ORDER OF PRECEDENCE. In the event of conflict between the Quote, a written agreement by MRP, and these Terms, the order of priority shall be: (1) the written

agreement by MRP, if only if executed by an MRP Officer, (2) the Quote and (3) these Terms, and only to the extent of the direct conflict. Notwithstanding the foregoing, MRP shall not be bound by, and specifically objects to, any terms, conditions or other provisions, both written and oral, which are different from, in addition to or inconsistent with the provisions of this Agreement which are set forth in any purchase order, receipt, acceptance, confirmation, correspondence or otherwise of, or by, Buyer. Fulfillment of Buyer’s order shall not constitute acceptance of any of Buyer’s terms and conditions and does not serve to modify or amend the terms and conditions contained herein.

        32.  SEVERABILITY. If any part of this Agreement is held to be void, illegal or unenforceable, then it shall be deemed to be severed from this Agreement and the remaining provisions shall continue in full force and effect; provided, however, that if any fundamental term or provision of this Agreement is held to be void, illegal or unenforceable, the remainder of this Agreement shall be unenforceable. Upon a determination that any term or provision is void, illegal or unenforceable, the parties shall negotiate in good faith to modify this Agreement to effect the original intent of the parties as closely as possible in order that the transactions contemplated hereby be consummated as originally contemplated to the greatest extent possible.