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How Single-Patient-Use Components Prevent Cross-Contamination in Medical Aesthetics

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Preventing cross-contamination in medical aesthetics depends heavily on how consistently clinics use single-patient-use components across injectable, laser, and energy-based procedures. Single-use tips, cannulas, syringes, tubing sets, and consumables create a physical and microbiological barrier that stops pathogens from traveling from one client to another, even when clinics are busy and patient turnover is high.

Understanding Cross-Contamination Risk in Medical Aesthetics

Medical aesthetics procedures frequently break the skin barrier through injections, microneedling, laser resurfacing, and minor surgical interventions, which exposes dermal and subdermal tissue to microorganisms from the environment, staff, and devices. When the same instrument, vial access needle, or treatment handpiece component makes contact with more than one patient without proper sterilization or replacement, there is a clear opportunity for cross-contamination and healthcare-associated infections.

Even low-risk treatments in med spas, dermatology clinics, and plastic surgery centers can become high-risk when microtrauma, bleeding, or contact with mucous membranes is involved. Pathogens of concern include gram-positive and gram-negative bacteria, viruses such as hepatitis B, hepatitis C, and HIV, as well as atypical mycobacteria and biofilm-forming organisms associated with dermal filler complications. In busy medical spa environments, short appointment times, staff turnover, and treatment volume magnify the importance of system-level infection prevention strategies.

What Single-Patient-Use Components Are in Aesthetic Practice

Single-patient-use components are devices or consumables designed to be used on only one individual and then discarded after that patient encounter. In medical aesthetics, these components span a wide range of product categories and are integral to injections, energy-based treatments, skin resurfacing, and support procedures.

Common single-patient-use items in aesthetic medicine include hypodermic needles, microcannulas for dermal fillers, microneedling cartridges, syringe tips, IV and infusion sets, tourniquets, adhesive tapes dedicated to one client, suction tubing segments, patient eye shields, and barrier sheaths for handpieces. Single-dose vials, disposable caps, and separate vial access needles are also part of the single-patient-use ecosystem that protects injectable medications and fillers from contamination during treatment.

How Single-Patient-Use Components Interrupt Transmission Pathways

Single-patient-use components break the chain of infection by eliminating shared fomites, which are surfaces and tools that can carry microorganisms between people. When a cannula, needle, or microneedling tip is dedicated to one client, any bacteria or viruses introduced onto that component remain confined and cannot be transmitted to another patient because the component is discarded immediately after use.

Single-use accessories also prevent cross-contamination in less obvious ways, such as stopping backflow of blood or tissue fluid into tubing or device channels that might otherwise be difficult to reprocess. By designing components that are exposed to blood or tissue to be single-patient-use only, manufacturers and clinics reduce reliance on complex reprocessing workflows and minimize the risk of residual contamination due to human error, incomplete sterilization, or incompatible device design.

Single-Use Needles, Cannulas, and Dermal Filler Safety

Needles and blunt-tip microcannulas used for dermal filler injections are a critical focus for infection control in aesthetic medicine. Injections frequently pass through the epidermis, dermis, and sometimes along periosteum, so any contaminant on the surface of a needle or cannula can be introduced into deeper tissues or existing filler material, where biofilms may form and trigger chronic inflammation or nodules.

When needles or cannulas are designated as single-patient-use, they are removed from the treatment field after that client’s injections and cannot serve as a vehicle for microorganisms to reach another patient. In vitro research has shown that dermal filler material can support bacterial biofilm formation once seeded, which makes preventing initial contamination especially important. Replacing cannulas and needles frequently during a single session, particularly after contacting bone or nonsterile surfaces, further reduces the risk of propagating bacteria along multiple injection points in the same patient.

Single-Dose Vials and Medication Handling in Aesthetic Clinics

Single-dose vials and proper vial access practices are another pillar of preventing cross-contamination in injectable aesthetics. Single-dose vials are manufactured and labeled for use on only one patient and one procedure, and the remaining contents are discarded afterward. This eliminates the risk of re-entering a vial with used needles or syringes and inadvertently introducing bloodborne pathogens or skin flora into the medication for later use.

When multi-dose vials must be used, infection control guidelines emphasize using a new needle and new syringe for every entry, never pooling leftover contents, and assigning vials to a single patient whenever feasible. In aesthetic medicine, where botulinum toxin, anesthetics, and other injectables are commonly employed, combining single-patient-use needles, syringes, vial access devices, and dedicated vials substantially decreases the likelihood of outbreaks tied to unsafe injection practices.

Disposable Tips and Barriers for Laser and Energy-Based Devices

Laser, IPL, RF microneedling, and ultrasound devices often rely on handpieces that come into close or direct contact with the skin. Single-patient-use tips, nozzles, cartridges, and protective sheaths prevent cross-contamination by ensuring that the part of the device touching the skin is either sterilized at manufacture or effectively isolated by a fresh barrier for each client.

In fractional laser and RF microneedling systems, disposable needle cartridges and treatment tips are a core infection prevention feature. They are individually packaged, sterile, and designed to be discarded immediately after a single patient’s session. For non-invasive handpieces, single-use plastic sheaths and barrier films prevent sweat, skin cells, and microorganisms from migrating into crevices or onto reusable surfaces that are difficult to disinfect between appointments, thereby lowering the risk of cross-contact between patients.

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Adhesive Tapes, Dressings, and Single-Patient-Use Rolls

Adhesive tapes, dressings, and bandages used after aesthetic procedures can act as high-risk fomites when shared between patients, especially because rolls of tape are rarely sterilized after opening. Evidence from acute-care environments has shown that dedicating a tape roll to a single high-risk patient or using short single-patient rolls significantly reduces opportunities for cross-contamination and infection.

In cosmetic dermatology and cosmetic surgery practices, switching to individually packaged dressings, single-patient rolls of tape, and dedicated wound-care kits minimizes the risk that residual blood, skin cells, or surface bacteria will transfer from one person’s postoperative site to another’s. This approach is particularly important after procedures such as ablative laser resurfacing, chemical peels, and minor surgical excisions where skin integrity is compromised.

Environmental Reservoirs and Single-Use Consumables in Med Spas

Airborne droplets, contaminated surfaces, and shared supplies can all contribute to microbial spread in medical spas. Single-patient-use consumables decrease the microbial load and duration of pathogen survival in the environment by shortening the lifespan of potential reservoirs. When gloves, gauze, cotton swabs, applicators, and barrier drapes are discarded immediately after patient contact, there are fewer objects in the room that can harbor microorganisms between appointments.

For example, pre-packaged IV start kits with short single-patient tape rolls and sterile disposables help staff avoid using shared rolls or open supplies left in treatment rooms. In aesthetic practices that offer IV vitamin drips, injectable weight-loss therapies, or regenerative medicine treatments, combining single-use tubing, connectors, and dressings with rigorous hand hygiene and surface disinfection generates a layered defense against infection.

Single-Patient-Use Versus Reusable Components: Risk and Reality

Reusable medical devices in aesthetics, such as metal handpieces and surgical instruments, can be safely employed when they undergo validated cleaning, disinfection, and sterilization cycles. However, real-world practice often reveals gaps related to time pressure, staff training, inadequate equipment, or complex device design, all of which can compromise reprocessing quality and allow residual contaminants to remain on instruments.

Single-patient-use components strategically remove the most challenging parts of the reprocessing chain by replacing them with sterilized, disposable alternatives. This is particularly valuable for high-risk components such as internal tubing, small-lumen channels, or complex microneedling cartridges that are difficult to clean. While reusable devices remain essential for many aesthetic surgery procedures, supplementing them with single-use accessories and patient-dedicated components offers a practical way to lower infection risk and standardize safety.

Regulatory and Guideline Perspectives on Disposable Devices

Healthcare regulators and infection control authorities consistently highlight single-use and single-patient-use devices as essential tools for preventing cross-transmission of pathogens. Guidelines in various medical domains emphasize that disposable devices intended for one patient should not be reprocessed, shared, or reused across encounters, especially if they contact blood, sterile tissue, or mucous membranes.

These guidelines are shaped by documented outbreaks associated with syringe reuse, improper vial handling, or inadequately reprocessed devices. In aesthetic medicine, aligning clinic policies with these standards means adopting single-patient-use needles, cannulas, vial access devices, tape rolls, and barrier tips for procedures that break the skin or contact non-intact tissue. Integrating such components into standard operating procedures demonstrates compliance with broader healthcare expectations for infection prevention.

Economic Impact and ROI of Single-Patient-Use Components

Clinic owners often weigh the cost of single-use components against perceived savings from reusing equipment or consumables. However, ROI calculations must account for the financial and reputational consequences of even a single infection event, which may involve treatment costs, legal exposure, loss of client trust, and negative reviews that reduce future revenue.

Investing in single-patient-use components can deliver positive ROI by reducing complications, minimizing downtime, and supporting premium positioning as a safety-focused medical aesthetic clinic. Lower rates of post-procedure infection or inflammatory complications translate into fewer follow-up visits for corrective care and more capacity for revenue-generating treatments. Over time, the consistent use of single-use components becomes a differentiator that supports client retention and referrals.

Real-World User Cases: Cross-Contamination and Prevention

Consider a hypothetical med spa that relies on shared tape rolls, multi-use microneedling tips, and ad hoc sterilization of accessory tubing between patients. Over several months, they notice an increased incidence of localized infections and prolonged erythema following microneedling and filler sessions. Investigations reveal inconsistent disinfection and occasional reuse of cartridges intended for single patients.

After transitioning to fully disposable microneedling cartridges, single-patient dressings, and dedicated tape segments in pre-packaged kits, the clinic observes a significant decline in infection-related callbacks and follow-up visits for inflammatory reactions. Another practice that standardizes single-patient-use cannulas and separate vial access needles reports fewer filler complications and a smoother patient journey, which translates into higher satisfaction scores and improved online reputation.

Company Background: ALLWILL’s Role in Safer Medical Aesthetics

ALLWILL is redefining B2B medical aesthetics by focusing on innovation, trust, and efficiency, helping clinics source, maintain, and upgrade devices with minimal operational friction. Through its Smart Center, MET vendor management system, and Lasermatch inventory platform, ALLWILL supports practitioners in choosing single-patient-use components and devices that align with rigorous performance, safety, and cost-optimization goals.

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Core Technology in Single-Use Aesthetic Components

The technology behind single-patient-use components in medical aesthetics has advanced beyond simple disposability. Modern microcannulas, syringe systems, and microneedling cartridges are engineered with precision manufacturing, high-quality stainless steel or medical-grade polymers, and surface treatments that improve glide, control, and patient comfort while maintaining sterility until opened.

Sterile barrier packaging and validation of sterilization processes ensure that each component reaches the treatment room free of viable microorganisms. In microneedling, for instance, disposable cartridges incorporate precise needle length control and integrated fluid channels while preventing backflow of blood into the handpiece. In laser and RF systems, some single-use tips incorporate RF contacts, insulation, and fluid interfaces that are designed for one patient’s energy delivery and then safely discarded.

Single-Patient-Use in RF Microneedling and Fractional Resurfacing

RF microneedling and fractional resurfacing procedures inherently create controlled micro-injuries in the skin, making infection prevention a top priority. Single-patient-use needle tips in these systems are designed with arrays that penetrate to calibrated depths, deliver energy, and then are safely removed and disposed after one session.

Because these tips contact blood and tissue, attempting to reprocess them would introduce substantial risk of incomplete decontamination, mechanical damage, and loss of sterility. Using fresh sterile tips for each patient prevents cross-contamination and preserves device performance, ensuring consistent energy delivery and penetration depth across treatments. This consistency also benefits clinical outcomes by maintaining predictable wound patterns and healing responses.

Single-Use Tourniquets, Gloves, and Ancillary Consumables

Although tourniquets and other ancillary accessories may seem low risk, they often contact skin, hair, and sweat and can act as reservoirs for microorganisms if reused across patients. Single-use tourniquets designed for one patient, combined with disposable gloves, gauze, and alcohol swabs, add layers to infection control protocols in aesthetic clinics that provide venipuncture, IV therapy, or injectable medications.

For example, a clinic offering IV hydration and regenerative therapies can use a new sterile tourniquet segment for each patient, dispose of it immediately after cannulation, and avoid the gradual contamination that occurs when reusable tourniquets are shared. Paired with proper hand hygiene and environmental disinfection, these consumables contribute to a comprehensive approach to reducing cross-contamination.

Building Protocols Around Single-Patient-Use Components

For single-patient-use strategies to be effective, clinics must integrate them into standardized protocols rather than relying on individual discretion. Written policies should specify which components are single-patient-use, how they are stored, how staff verify packaging integrity, and when they must be discarded.

Training should emphasize that single-patient-use items cannot be reprocessed, re-packaged, or used across different sessions, even if they appear clean or were used briefly. Inventory management systems can support adherence by ensuring adequate stock levels, avoiding situations where staff feel pressured to reuse items due to shortages. Clear labeling, color-coding, and tray organization further reduce errors and support consistent practices.

Competitor Comparison Matrix: Single-Use Strategy Approaches

Provider Model Single-Patient-Use Strategy Infection Control Strengths Typical Challenges
Traditional med spa using mixed reusable and disposable tools Selective use of single-use needles, shared tape rolls, limited disposable tips Lower upfront consumable cost, flexibility with existing devices Higher cross-contamination risk, variable staff compliance, reprocessing complexity
Premium safety-focused aesthetic clinic Broad use of single-patient-use needles, cannulas, tips, dressings, and tourniquets Strong infection prevention, simplified workflows, clear patient safety messaging Higher consumable spend, requires robust inventory planning
Device manufacturer with integrated disposable tip ecosystem Devices designed around proprietary single-use cartridges and tips Optimized performance, validated sterility, predictable per-treatment costs Dependence on manufacturer supply, need for long-term cost evaluation
Surgery-oriented aesthetic practice with central sterile department Reusable instruments plus selective single-use components for high-risk interfaces Strong sterilization infrastructure, tailored use of single-use accessories Complexity of managing both streams, higher training and documentation needs

Top Single-Patient-Use Component Types in Medical Aesthetics

Component Type Key Advantages Typical Ratings and Adoption Common Use Cases
Single-use needles and microcannulas Reduced cross-contamination, precise filler placement, minimal trauma Widely adopted in filler and toxin injections Dermal filler injections, neuromodulator injections, local anesthesia
Disposable microneedling cartridges Sterile needle arrays, controlled depth, no reprocessing required High adoption in professional microneedling systems Collagen induction therapy, scar remodeling, RF microneedling
Single-use laser and RF tips Clean patient interface, consistent energy delivery, reduced cleaning burden Moderate to high adoption depending on device family Fractional RF, fractional laser resurfacing, vaginal rejuvenation
Single-patient rolls of tape and dressings Lower risk of shared fomites, ease of post-procedure care Growing adoption in high-safety practices Post-laser dressings, peel recovery, minor procedure wound care
Single-patient tubing and IV sets Prevents backflow contamination, supports IV therapy safety Standard in IV-based services IV vitamin drips, regenerative infusions, sedation or analgesia support

Measuring Outcomes: Infection Reduction and Patient Confidence

To evaluate the impact of single-patient-use components, clinics can track metrics such as post-procedure infection rates, reported delayed inflammatory reactions, and the frequency of antibiotic prescriptions after aesthetic treatments. A downward trend in these indicators following the adoption of single-use systems is a strong signal of improved infection control.

Equally important is the effect on patient confidence and perceived quality. Clients increasingly research safety practices and ask about needle reuse, sterilization, and clinic hygiene. When staff can confidently explain that needles, cannulas, cartridges, and dressings are all single-patient-use, it reinforces trust and differentiates the clinic from competitors that cannot articulate such standards as clearly.

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Training Clinical Teams on Single-Patient-Use Best Practices

Even the most advanced single-use components cannot prevent cross-contamination if staff are unaware of proper handling practices. Training should cover aseptic technique, correct donning and removal of gloves, how to open sterile packaging without contaminating the contents, and how to dispose of sharps and biohazard waste safely.

Simulation-based training, checklists, and periodic audits help identify gaps in practice, such as inadvertently touching sterile needle hubs or placing sterile tips on non-sterile trays. Understanding why certain items are single-patient-use and how they support patient safety encourages team buy-in and reduces the temptation to deviate from protocols when under time pressure.

Environmental Sustainability and Single-Use Components

One concern with single-patient-use devices is their environmental footprint, particularly increased medical waste. In aesthetic medicine, clinics can address this by working with suppliers that optimize packaging, reduce unnecessary plastics, and participate in responsible waste-handling programs in compliance with local regulations.

Balancing sustainability with infection prevention requires a risk-based approach: prioritize single-patient-use for high-risk interfaces that contact blood, non-intact skin, or sterile tissue, and consider reusable options with validated sterilization protocols for lower-risk accessories where appropriate. Some manufacturers are exploring recyclable packaging or materials that maintain sterility while reducing environmental impact, which may become more mainstream in the coming years.

Aligning Marketing and Patient Education With Safety Practices

Marketing messages and patient education materials should accurately reflect the clinic’s commitment to infection prevention and the use of single-patient-use components. Rather than generic claims about cleanliness, clinics can explain that every client receives new sterile needles, cannulas, microneedling tips, and dressings as part of standard care.

In pre-treatment consultations, practitioners can highlight safety procedures alongside treatment benefits and expected outcomes. When patients understand that a portion of their treatment fee supports single-patient-use safety measures and high-quality consumables, they are more likely to perceive the service as premium and justified in cost, enhancing acceptance and long-term loyalty.

Three-Level Conversion Funnel CTA for Safety-Focused Clinics

At the awareness stage, aesthetic practices can publish educational content explaining how single-patient-use components protect clients from cross-contamination and why this matters for fillers, neurotoxins, microneedling, and laser treatments. This helps prospective patients recognize safety as a defining quality metric when choosing a provider.

At the consideration stage, clinics can invite interested prospects to schedule in-person or virtual consultations that include a transparent walkthrough of treatment-room safety protocols, showing sealed needles, disposable tips, and single-patient kits before each procedure. At the decision stage, front-desk and clinical staff can reinforce this safety narrative during booking and consent, reminding patients that each treatment includes fresh, sterile, single-patient-use components tailored to their procedure.

Future Trends in Single-Patient-Use Components for Aesthetic Medicine

Future developments in single-patient-use technology are likely to focus on smart packaging, integrated traceability, and device ecosystems built around plug-and-play disposable cartridges. Serialization and digital tracking of single-use tips, cannulas, and cartridges may allow clinics to document exactly which components were used for each treatment, improving quality control and medico-legal documentation.

We can also expect more device manufacturers to design aesthetic platforms that rely on proprietary single-use modules optimized for energy delivery, cooling, and tissue interaction, ensuring consistent performance with each new component. As regulatory expectations around infection control continue to escalate, clinics that adopt comprehensive single-patient-use strategies now will be better positioned to meet future standards while offering patients safer, more predictable outcomes.

Relevant FAQs on Single-Patient-Use Components and Cross-Contamination

What is the difference between single-use and single-patient-use components in aesthetics?
Single-use components are intended for one procedure on one patient and must be discarded afterward, while single-patient-use components may be reused on the same individual across a treatment course but never shared with another patient.

Why are single-patient-use cannulas and needles essential in dermal filler treatments?
They prevent blood, skin flora, and environmental microorganisms from being carried from one client to another and reduce the chance of seeding bacteria into filler material, which can lead to biofilm formation and chronic complications.

Can reusable instruments be as safe as single-patient-use components?
Reusable instruments can be very safe when processed through validated sterilization cycles with strict adherence to guidelines, but single-patient-use components eliminate many reprocessing variables and human-factor errors.

How should aesthetic clinics dispose of single-patient-use components?
Sharps such as needles and cannulas should go into approved sharps containers, while other contaminated disposables should be placed in biohazard waste according to local infection control and environmental regulations.

Do single-patient-use components increase treatment costs for patients?
They add a consumable cost to each procedure, but this is offset by lower infection rates, fewer complications, stronger patient trust, and a clear safety advantage that supports premium positioning for the clinic.

By adopting a structured single-patient-use strategy across needles, cannulas, cartridges, dressings, tubing, and ancillary supplies, medical aesthetic practices can significantly reduce cross-contamination risks, enhance patient outcomes, and build a defensible reputation for safety in an increasingly competitive market.

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(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.