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What Are Disposable Probes for Advanced Aesthetic Technologies?

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Disposable probes for advanced aesthetic technologies are single‑use applicators that interface directly with energy‑based devices—such as radiofrequency (RF), ultrasound, or laser systems—to deliver precise, controlled treatments while minimizing cross‑contamination and downtime between patients. These probes are engineered to maintain consistent performance across a single procedure, then be safely discarded, which reduces infection risk, simplifies sterilization logistics, and supports higher throughput in busy clinics. For practices investing in high‑end aesthetic platforms, pairing them with compatible disposable probes—sourced through partners such as ALLWILL—helps protect both device longevity and patient safety.

How Is the Aesthetic Device Market Changing?

The global aesthetic medical devices market is projected to grow from roughly $15–16 billion in 2023 to over $25 billion by 2030, reflecting strong demand for minimally invasive and non‑surgical treatments. As more clinics adopt advanced platforms (RF, ultrasound, microneedling, and fractional lasers), operators face pressure to treat more patients per day while complying with stricter infection‑control and regulatory standards.

At the same time, recent clinical and regulatory discussions emphasize that reusable handpieces and probes can harbor biofilm and cross‑contamination if not cleaned and sterilized perfectly every time. A single lapse can trigger patient‑safety incidents, regulatory citations, or reputational damage—costs that far exceed the price of consumables.

Why Are Reusable Probes a Growing Liability?

Reusable probes require meticulous cleaning, high‑level disinfection, and often autoclaving between patients, yet studies of medical‑device reprocessing show that up to 20–30% of reprocessed instruments fail cleanliness benchmarks in real‑world settings. In aesthetic clinics, where treatment rooms turn over rapidly and staff may lack formal sterile‑processing training, this gap translates into tangible infection‑risk exposure.

Another hidden cost is device wear. Each reprocessing cycle subjects metal and electronic components to thermal, chemical, and mechanical stress, which can degrade calibration, sensor accuracy, and RF‑energy delivery over time. Clinics that rely on aging, heavily reused probes often see inconsistent treatment outcomes, more frequent recalibration, and higher repair or replacement bills—issues that ALLWILL addresses through its refurbished‑device and vendor‑management ecosystem.

What Problems Do Disposable Probes Solve?

Disposable probes are designed to be used once per patient and then discarded, removing the need for in‑clinic reprocessing altogether. Because each probe is factory‑sterilized and pre‑calibrated, clinics gain:

  • Consistent energy delivery across treatments, since there is no cumulative wear from repeated sterilization.

  • Reduced infection risk, because contaminated or inadequately cleaned probes are no longer a factor.

  • Faster room turnover, since staff skip reprocessing steps and move directly to the next patient.

For practices that source their aesthetic platforms through ALLWILL, integrating disposable probes also aligns with the company’s focus on reliability, data‑driven maintenance, and minimizing downtime.​

What Are the Limitations of Traditional Reusable Probes?

Traditional reusable probes are typically made of metal or rigid polymers with embedded sensors and connectors, built to withstand hundreds of sterilization cycles. In theory, this reduces consumable costs; in practice, it introduces several weaknesses:

  • Inconsistent performance over time, as repeated heat and chemical exposure dull sensors and alter thermal‑conductivity characteristics.

  • Higher labor and compliance burden, because every probe must be logged, cleaned, disinfected, and often tested for integrity.

  • Greater risk of cross‑contamination, especially when clinics skip steps or use suboptimal cleaning agents.

Also check:  Elevate Your Medical Aesthetics Practice with ALLWILL Training and Support

These drawbacks become especially problematic in multi‑provider practices where different staff members handle reprocessing, increasing variability in how well probes are maintained.

What Are Disposable Probes and How Do They Work?

Disposable probes for advanced aesthetic technologies are typically lightweight, single‑use applicators that plug into an RF, ultrasound, or laser generator and deliver energy through a controlled tip or array. Many modern disposable RF probes, for example, feature:

  • Reinforced, color‑coded cables that simplify length selection and reduce tripping hazards.

  • Pre‑calibrated sensors that ensure the device “sees” the same impedance and temperature profile on every use.

  • Single‑patient‑use design, so the probe is discarded immediately after treatment and replaced for the next patient.

Because the probe is never reprocessed, the clinic avoids the variability introduced by cleaning, drying, and sterilization, which in turn supports more predictable clinical outcomes and fewer callbacks or touch‑ups.

How Do Disposable Probes Compare with Reusable Probes?

The table below contrasts traditional reusable probes with modern disposable probes in key operational dimensions.

Dimension Traditional Reusable Probes Disposable Probes
Sterilization burden High; requires cleaning, disinfection, and often autoclaving between patients None; factory‑sterilized, single‑use
Infection‑risk exposure Moderate–high if reprocessing is inconsistent Very low; no shared‑patient hardware
Performance consistency Declines over time due to wear and repeated sterilization Stable; each probe is new and pre‑calibrated
Staff time per patient Additional minutes for cleaning and logging No extra reprocessing time; plug‑and‑treat workflow
Upfront cost per probe Lower per‑unit purchase price Higher per‑unit consumable cost
Long‑term maintenance cost Higher due to repairs, recalibration, and eventual replacement Lower, since the generator and handpiece are protected from probe‑level wear

Clinics that partner with ALLWILL can offset higher per‑probe costs by selecting refurbished or trade‑up‑eligible aesthetic platforms, which lowers the total‑cost‑of‑ownership while still enabling a disposable‑probe workflow.​

How Do You Implement Disposable Probes in a Clinic?

Integrating disposable probes into an advanced aesthetic practice follows a straightforward, repeatable workflow:

  1. Select compatible probes and devices
    Match the disposable‑probe model to the generator (e.g., RF or ultrasound platform) and confirm compatibility with the clinic’s existing or planned equipment. ALLWILL offers brand‑agnostic consultations that help operators choose probe‑generator pairs that align with their budget and clinical goals.

  2. Establish a supply‑chain routine
    Set minimum inventory levels and reorder points so probes never run out during peak‑treatment days. Practices using ALLWILL’s inventory platform, Lasermatch, can track probe usage and automate replenishment more efficiently.

  3. Train staff on plug‑and‑dispose workflow
    Teach providers and nurses how to attach the probe, run a quick system check, treat the patient, and then safely discard the probe into designated medical‑waste containers.

  4. Update SOPs and compliance documentation
    Revise infection‑control protocols to reflect the shift from reusable to disposable probes, and document training and probe‑usage logs for audits.

  5. Monitor outcomes and cost per treatment
    Track treatment times, patient‑satisfaction scores, and repair incidents over 3–6 months to quantify the impact of disposable probes on efficiency and device reliability.

Where Do Disposable Probes Deliver the Most Value?

1. High‑Volume Medical Spas

Problem: Busy medical spas often treat 15–20 patients per day with RF tightening, skin‑tightening, or body‑contouring protocols. Reusable probes require frequent reprocessing, which slows room turnover and increases staff workload.

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Traditional practice: Staff clean and disinfect probes between patients, sometimes rushing steps during peak hours.

With disposable probes: Each patient receives a new, factory‑sterilized probe; room turnover improves by 10–15%, and infection‑control audits show fewer non‑compliance findings.

Key benefit: Higher throughput without sacrificing safety, which directly boosts revenue per square foot.

2. Multi‑Provider Aesthetic Clinics

Problem: In clinics with several physicians or nurse practitioners, probe‑handling practices vary, leading to inconsistent cleaning and calibration drift.

Traditional practice: Probes are shared across providers, with reprocessing logs that are sometimes incomplete or inaccurate.

With disposable probes: Each provider uses a fresh probe per patient, eliminating shared‑probe variability and simplifying accountability.

Key benefit: More consistent clinical outcomes and fewer device‑related callbacks, which supports stronger patient‑retention rates.

3. Mobile or Pop‑Up Aesthetic Services

Problem: Mobile aesthetic providers operate in non‑sterile environments and lack access to hospital‑grade sterilization equipment.

Traditional practice: Reusable probes must be transported, cleaned in suboptimal conditions, and often reprocessed off‑site, increasing risk and logistical complexity.

With disposable probes: Providers carry a stock of single‑use probes and discard them after each treatment, relying on factory‑sterilized units rather than field‑level reprocessing.

Key benefit: Safer, more compliant operations in non‑traditional settings, which is critical for maintaining licensure and insurance coverage.

4. Clinics Using High‑End RF Platforms

Problem: Premium RF platforms are expensive to purchase and maintain; probe‑level wear can trigger costly recalibrations or repairs.

Traditional practice: Clinics reuse probes for hundreds of treatments, accepting gradual performance degradation to save on consumables.

With disposable probes: Each treatment starts with a fresh, pre‑calibrated probe, protecting the generator and extending the platform’s service life.

Key benefit: Lower lifetime maintenance costs and fewer unplanned downtimes, which aligns with ALLWILL’s mission of optimizing performance while reducing total‑cost‑of‑ownership.​

When Will Disposable Probes Become the Standard?

Disposable probes are already common in interventional and surgical fields (e.g., RF ablation, endoscopic tools), and regulatory bodies increasingly favor single‑use designs where feasible. As aesthetic medicine matures into a more regulated specialty, expect:

  • Stricter reprocessing requirements for reusable probes, raising compliance costs.

  • More probe‑generator platforms designed from the outset for disposable applicators, not just retrofitted options.

  • Greater emphasis on traceability, with serialized disposable probes that can be linked to patient records and treatment logs.

Clinics that adopt disposable‑probe workflows now position themselves ahead of these shifts, reducing future retrofit costs and regulatory risk. ALLWILL’s vendor‑management system, MET, can connect practices with technicians and trainers who specialize in disposable‑probe‑enabled platforms, ensuring smooth transitions as the market evolves.

FAQ

What Are Disposable Probes for Advanced Aesthetic Technologies?
Disposable probes are single-use tips designed for aesthetic devices, enhancing hygiene, safety, and treatment precision. They prevent cross-contamination and ensure consistent results for procedures like microneedling, RF, and laser treatments. Using disposable probes protects both patients and practitioners while improving efficiency and clinical outcomes.

How Do Disposable Probes Improve Safety in Aesthetic Treatments?
Disposable probes reduce the risk of infection and cross-contamination in aesthetic clinics. By eliminating the need for sterilization between uses, they maintain a consistent hygiene standard, improve patient trust, and comply with regulatory safety requirements. Clinics adopting disposable probes enhance treatment safety and reliability.

Also check:  How to nail preventive maintenance for medical aesthetic devices?

Which Disposable Probes Work Best with RF Microneedling Devices?
For RF microneedling, probes with precise conductivity, adjustable depth, and ergonomic design are ideal. Look for high-quality materials that maintain consistent energy delivery for skin rejuvenation. Choosing the right probe ensures maximum patient comfort and optimal clinical results. ALLWILL offers guidance on compatible, reliable options for every device.

How Much Do Disposable Probes for Aesthetic Technologies Cost?
Disposable probe costs vary depending on device compatibility, material, and brand. Clinics can manage expenses by buying in bulk, using trade-up programs, or sourcing from trusted vendors. Proper cost planning ensures high-quality treatments without overspending. ALLWILL provides pricing insights and budget-friendly procurement solutions for practitioners.

What Are the Different Types of Disposable Probes for Skin Treatments?
Disposable probes include microneedling, RF, laser, ultrasound, cryotherapy, vacuum-assisted, and combined multi-function probes. Each type targets specific skin concerns, such as collagen stimulation, wrinkle reduction, or fat reduction, allowing practitioners to customize treatments and improve results for diverse patient needs.

What Are the Best Practices for Using Disposable Probes in Aesthetic Clinics?
Always use probes once, follow device manufacturer guidelines, and dispose safely after treatment. Store in a clean environment and check compatibility before use. Proper handling enhances safety, prolongs device life, and ensures predictable treatment outcomes for every patient.

Who Are the Leading Suppliers of Disposable Probes for Aesthetic Clinics?
Leading suppliers provide reliable, high-quality disposable probes with broad device compatibility. Look for vendors offering training, technical support, and consistent supply. ALLWILL connects clinics to vetted suppliers and ensures probes meet rigorous performance and safety standards.

Are There Eco-Friendly Options for Disposable Probes in Aesthetic Technologies?
Yes, some disposable probes are biodegradable or recyclable, reducing environmental impact while maintaining hygiene and treatment efficiency. Clinics seeking sustainable alternatives can adopt these eco-conscious options without compromising patient safety or clinical outcomes.

Disposable probes for advanced aesthetic technologies are no longer a niche option; they are becoming a practical necessity for clinics that prioritize patient safety, regulatory compliance, and operational efficiency. By shifting from reusable to disposable applicators, practices reduce infection‑risk exposure, stabilize treatment outcomes, and protect their high‑value aesthetic platforms from unnecessary wear.

For operators evaluating new or refurbished devices, ALLWILL offers a complete ecosystem—from device sourcing and refurbishment to vendor‑managed training and probe‑compatible workflows—that makes it easier to adopt disposable‑probe‑enabled technologies without overextending budgets. If you are ready to modernize your aesthetic practice, contact ALLWILL today to schedule a brand‑agnostic consultation and explore how disposable probes can integrate seamlessly into your current or future device lineup.​

References

  1. Epimed – Disposable RF™ Probes product page
    https://epimed.com/product/disposable-rf-probes/​

  2. Epimed – Disposable RF™ Probes product listing (alternative page)
    https://shop.epimed.com/product/disposable-rf-probes/​

  3. Advanced Aesthetic Technologies Inc. – Company overview
    https://www.algeness.com/about-us-advanced-aesthetic-technologies.html​

  4. Nevada Department of Health and Human Services – Disposable blade‑head requirements
    https://www.leg.state.nv.us/Division/Research/Documents/RTTL_NRS439.877_2025_SNAMHS.pdf​

  5. PubMed – Clinical use of disposable decomposing soft injection probe
    https://pubmed.ncbi.nlm.nih.gov/40707371/​

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        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.