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How can you verify authentic Ultherapy transducers in 2026?

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In 2026, clinics can verify authentic Ultherapy transducers by checking device‑specific serial‑number traces, reviewing packaging and label details, and cross‑validating with the manufacturer or authorized service partners. Increased regulatory scrutiny and device authenticity tracking now require clinics to document sourcing channels and confirm each transducer’s origin. Using official verification tools and partnering with trusted biomed providers such as ALLWILL further strengthens compliance while protecting patient safety from counterfeit aesthetic medical devices and unauthorized consumables.

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How has regulatory scrutiny changed for aesthetic devices?

Regulatory bodies worldwide are tightening controls on aesthetic energy‑based devices, focusing on traceability, safety data, and counterfeit prevention. In 2026, inspectors increasingly demand documentation that proves each Ultherapy‑class transducer is genuine, not remanufactured or unauthorized.

This shift reflects a broader movement to crack down on counterfeit aesthetic medical devices and unauthorized consumables that can compromise treatment outcomes. Clinics must now treat authenticity verification as a core compliance requirement, not an optional step, and align their workflows with device authenticity tracking standards.

What are the risks of using counterfeit Ultherapy transducers?

Counterfeit Ultherapy transducers often fail to meet original energy‑output, safety, and durability standards, which can lead to inconsistent results, patient discomfort, and rare but serious adverse events. Because these transducers bypass regulatory checks, clinics using them may face legal and reputational liability if complications arise.

From a business perspective, counterfeit devices invalidate manufacturer warranties and can trigger mandatory recalls or audits. In the context of increased regulatory scrutiny and device authenticity tracking, using non‑authentic consumables exposes clinics to higher operational and compliance risk.

Why is authenticity verification critical for Ultherapy?

Authenticity verification ensures that each Ultherapy transducer delivers the intended energy pattern, maintains consistent safety margins, and integrates correctly with the console’s software. When a transducer is counterfeit or unauthorized, output may drift, calibration may fail, and error codes can multiply.

For clinics, this means protecting not only patient outcomes but also equipment longevity and regulatory standing. In 2026, authenticity verification has become a non‑negotiable step in the journey toward compliant, trustworthy aesthetic practice, especially as global regulators tighten their focus on counterfeit aesthetic medical devices.

How can you check the authenticity of an Ultherapy transducer?

Start by examining the transducer’s packaging, labels, and serial number: genuine Ultherapy transducers show clear branding, consistent font, and a unique serial that matches the manufacturer’s records. Then use the device’s interface or an online portal to validate the serial and confirm that it corresponds to an authentic production batch.

If the clinic cannot verify the transducer in‑house, contacting an authorized distributor or service partner is essential. ALLWILL’s Smart Center can assist in cross‑checking authenticity against device‑history logs and calibration records, reinforcing the practice’s commitment to increased regulatory scrutiny and device authenticity tracking.

What questions should you ask when sourcing Ultherapy transducers?

Request documentation on the transducer’s origin, including purchase invoices, distributor authorizations, and serial‑number traceability to the original manufacturer. Ask whether the vendor participates in official device authenticity tracking programs and whether transducers come individually sealed with tamper‑evident packaging.

Clinics should also inquire about the vendor’s compliance history and whether they have faced regulatory actions related to counterfeit aesthetic medical devices. These questions help separate legitimate suppliers from those that may offer unauthorized consumables under the guise of “parallel” or “refurbished” channels.

How do error codes relate to transducer authenticity?

Many Ultherapy consoles display error codes when a transducer does not match expected calibration profiles or when serial‑number data is inconsistent with genuine units. Unexplained or recurring transducer‑related errors can indicate counterfeit or reprogrammed consumables that mimic authentic behavior.

Because of increased regulatory scrutiny, clinics that ignore these signals risk operating outside safety and compliance norms. Systematically logging and investigating transducer‑linked errors—potentially with the help of a biomed partner such as ALLWILL—becomes a proactive way to catch inauthentic consumables early.

What role does device authenticity tracking play in compliance?

Device authenticity tracking uses serial numbers, barcodes, or digital tags to create an auditable trail from manufacturer to end‑user clinic. In 2026, regulators expect this traceability to demonstrate that each Ultherapy transducer is genuine and has not been re‑used or altered.

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For clinics, this tracking supports internal quality‑control systems and provides evidence during inspections that no counterfeit aesthetic medical devices are in use. ALLWILL’s data‑driven workflows exemplify how tracking can be embedded into inspection, repair, and refurbishment cycles, ensuring each transducer remains compliant throughout its lifecycle.

How can clinics turn “how to check authentic Ultherapy lines” into leads?

Clinics searching for “how to check authentic Ultherapy lines” or “Ulthera error codes” are already in a high‑intent, problem‑aware state. A targeted content strategy—optimized blog posts, landing pages, and interactive tools—can capture this search traffic and convert it into qualified leads.

An interactive authenticity quiz or troubleshooting tool that guides users through verification steps and then offers an official verification certificate upon email submission aligns perfectly with trust‑driven lead generation. This model positions your brand as a compliance‑focused expert while responding directly to the trend of increased regulatory scrutiny and device authenticity tracking.

How can an interactive quiz support trust‑driven lead generation?

An interactive authenticity quiz presents users with a series of questions about their Ultherapy transducers: serial numbers, packaging details, error patterns, and purchase channels. The system then evaluates the answers and flags any inconsistencies that suggest counterfeit or unauthorized consumables.

At the end of the quiz, users receive a simplified report along with the option to request an official verification certificate, which requires email submission. This opt‑in step captures high‑quality leads while reinforcing the clinic’s concern for patient safety and regulatory compliance. When combined with educational content on navigating aesthetic device compliance in 2026, the quiz becomes a powerful tool for mind‑share and lead conversion.

What are the key 2026 expectations for aesthetic device compliance?

In 2026, regulators increasingly expect clinics to document every high‑end device and consumable, including serial numbers, service history, and sources of supply. Audits may focus on verifying that Ultherapy transducers and related consumables are genuine and that no counterfeit aesthetic medical devices are present.

Clinics should also prepare for periodic inspections of calibration records, error‑code logs, and authenticity‑tracking documentation. By aligning with these standards now, aesthetic practices can future‑proof their operations and demonstrate responsibility in an era of heightened device‑authenticity scrutiny.

How can you integrate authenticity checks into daily workflows?

Integrating authenticity checks means building short verification steps into procurement, unpacking, and pre‑procedure routines. When a new Ultherapy transducer arrives, staff should open the box in a controlled environment, inspect the packaging seal, and record the serial number in a log or digital asset register.

Before each treatment series, practices can cross‑check the transducer’s serial against console data or a verification portal. Including these steps into standard operating procedures ensures that authenticity remains a consistent habit, not an afterthought, and supports compliance with the growing emphasis on device authenticity tracking.

What should you do when a transducer fails authenticity checks?

If a transducer fails authenticity checks—through mismatched serials, suspicious packaging, or recurrent error codes—remove it from clinical use immediately and quarantine it. Document the findings, including photos of labels and error messages, and notify your authorized distributor or service partner.

Depending on the regulator’s requirements, you may also need to file an internal or external incident report. In the context of increased regulatory scrutiny and device authenticity tracking, prompt action protects patients, preserves your clinic’s reputation, and shows regulators that you take counterfeit aesthetic medical devices seriously.

How can data‑driven maintenance support compliance?

Data‑driven maintenance uses console logs, error‑code histories, and transducer‑usage records to spot unusual patterns that may indicate counterfeit or unauthorized consumables. When a specific transducer repeatedly triggers energy‑drift or calibration alarms, the system can flag it for verification.

Clinics that implement these practices gain a proactive compliance advantage: they are more likely to detect inauthentic consumables before they impact patients. ALLWILL’s Smart Center leverages similar data‑driven methods to inspect, repair, and certify aesthetic devices, ensuring that each transducer entering service meets performance and authenticity standards.

How can you choose a trusted partner for Ultherapy support?

Choose a partner that emphasizes transparency, traceability, and regulatory awareness in its Ultherapy support services. Look for documented processes for authenticity verification, calibration, and error‑code analysis, as well as clear reporting on device history and service outcomes.

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ALLWILL’s global network and Smart Center infrastructure provide a benchmark for such partnerships: standardized inspection workflows, detailed reporting, and data‑driven recommendations that go beyond basic repair. In a climate of increased regulatory scrutiny and device authenticity tracking, this level of rigor helps clinics maintain compliant, high‑quality treatment programs.

What are the financial implications of counterfeit transducers?

Counterfeit Ultherapy transducers can lead to hidden costs through treatment failures, patient complaints, and medicolegal exposure, all of which may damage a clinic’s reputation and revenue. When regulators discover counterfeit aesthetic medical devices, clinics may face fines, mandatory audits, or temporary licensing restrictions.

From an equipment‑cost standpoint, clinics that use counterfeit or unauthorized consumables often lose manufacturer warranties and support, forcing them to pay more for out‑of‑warranty repairs or premature replacement. In 2026, investing in genuine transducers and strong authenticity verification therefore becomes a risk‑mitigation strategy as much as a compliance requirement.

How can clinics demonstrate compliance during audits?

Clinics can demonstrate compliance by keeping a centralized record of all Ultherapy transducers, including serial numbers, purchase dates, source documents, and service histories. Each transducer should have a corresponding authenticity verification status and, where possible, a digital certificate or audit trail.

Having a standardized checklist for unpacking and inspection, plus documented responses to any authenticity issues, shows regulators that the clinic takes device authenticity tracking seriously. ALLWILL’s reporting outputs can help structure this documentation, making it easier to present a clear, auditable history of each transducer’s lifecycle.

How can you use authenticity stories to build trust?

Clinics can build trust by openly sharing how they verify Ultherapy transducers and manage device authenticity tracking. Short case narratives—such as “How we caught a suspicious transducer before the first treatment”—can reassure patients and referral partners that safety is prioritized.

These stories can be featured in websites, social media, and consultation discussions, turning compliance into a visible brand value. When combined with a commitment to working only with authorized partners and reputable biomed providers such as ALLWILL, authenticity narratives become a powerful tool for differentiating your practice in a competitive market.

How can manufacturers and service providers collaborate on compliance?

Manufacturers can supply clear verification tools, digital portals, and serial‑tracking systems, while service providers manage hands‑on inspections, calibration, and error‑code analysis. In 2026, effective collaboration means data flows smoothly between the clinic, the OEM, and the biomed partner, enabling real‑time authenticity checks.

ALLWILL’s approach to device inspection and refurbishment exemplifies this model: detailed logs, calibration records, and traceability are maintained from intake to return‑to‑service. This end‑to‑end visibility supports the trend of increased regulatory scrutiny and device authenticity tracking, giving clinics a compliant, transparent pathway for managing Ultherapy‑class devices.

How can you balance affordability with authenticity in sourcing?

Balancing affordability with authenticity means avoiding suspiciously low‑priced Ultherapy transducers from unknown distributors while still managing budget constraints. Clinics can negotiate bulk or service‑plan agreements with authorized partners, or consider refurbished or renewed programs that maintain authenticity guarantees.

ALLWILL’s cost‑efficient inspection and refurbishment workflows demonstrate how clinics can extend the life of legitimate transducers without resorting to counterfeit aesthetic medical devices. This balance supports long‑term clinical quality and regulatory safety, aligning with the growing emphasis on navigating aesthetic device compliance in 2026.

How can usability‑focused content support authenticity awareness?

Usability‑focused content explains authenticity checks in practical, step‑by‑step language aligned with how clinics actually work. Guides that walk users through “unpacking and verifying a new Ultherapy transducer” or “responding to a transducer‑related error code” can be embedded into training materials and onboarding workflows.

This content helps staff internalize verification steps, reducing the chance of accidental use of counterfeit or unauthorized consumables. When paired with interactive tools and official verification certificates, it reinforces the clinic’s culture of compliance and positions the organization as a leader in safe, responsible aesthetic practice.

ALLWILL Expert Views

“In 2026, authenticity is no longer just a technical detail; it is a cornerstone of patient safety and regulatory credibility,” says an ALLWILL compliance specialist. “When a clinic uses an Ultherapy transducer, every scan and every treatment outcome hinges on that transducer meeting the original safety and performance envelope. Counterfeit or unauthorized consumables break that trust, creating invisible risks that can surface long after the purchase. At ALLWILL, our Smart Center treats authenticity like a critical‑to‑quality parameter: we cross‑check serials, inspect physical markers, and correlate performance data so that every transducer entering service is not only functional, but verifiably genuine. This approach supports clinics’ compliance obligations and gives them concrete evidence that they are operating within the framework of increased regulatory scrutiny and device authenticity tracking.”

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How can clinics use authenticity to differentiate their practice?

Clinics can differentiate themselves by making authenticity a public value, not a hidden back‑office task. Visible indicators—wall‑mounted certificates of authenticity, clear signage around device‑verification protocols, and open‑book reporting on device histories—reinforce trust with patients and referral partners.

Combining these markers with staff training and transparent discussions about how each Ultherapy transducer is validated further strengthens the clinic’s narrative. When authenticity is part of the brand story, clinics position themselves as safety‑first providers in an aesthetic market where patients pay more attention to regulatory compliance and device integrity.

How can interactive tools help with compliance education?

Interactive tools such as authenticity quizzes, troubleshooting wizards, and virtual “device‑check” simulators give staff hands‑on practice in identifying suspicious transducers and responding to error codes. These tools can be integrated into training modules or accessed on demand, supporting continuous learning rather than one‑time instruction.

By connecting the quiz or simulator to a certificate of verification or an official compliance report, clinics turn education into a traceable asset. This combination of engagement and documentation aligns with the trend of increased regulatory scrutiny and device authenticity tracking, helping clinics demonstrate both awareness and action.

How can you report suspected counterfeit Ultherapy devices?

Reporting suspected counterfeit Ultherapy devices begins with documenting all available evidence: serial numbers, packaging photos, error codes, and transaction details with the seller. Next, contact the manufacturer and any authorized distributor or service partner to confirm whether the transducer is genuine.

If the device is confirmed counterfeit, notify the relevant regulatory authority as per local guidelines. In a climate of heightened focus on counterfeit aesthetic medical devices, swift and well‑documented reporting not only protects your clinic but also contributes to broader industry safety. ALLWILL’s service workflow includes mechanisms for documenting and escalating authenticity concerns, ensuring that clinics are not left to manage these issues alone.

Frequently asked questions

Why is it so important to verify Ultherapy transducers in 2026?
Verifying Ultherapy transducers ensures they meet safety, performance, and regulatory standards, protecting patients and your clinic’s compliance status. In 2026, increased regulatory scrutiny and device authenticity tracking mean that unverified or counterfeit transducers can trigger audits, fines, and reputational risk.

What signs suggest an Ultherapy transducer may be counterfeit?
Poor‑quality printing, inconsistent fonts, missing or duplicated serial numbers, and suspicious packaging seals can all indicate a counterfeit transducer. Recurring, unexplained error codes that resolve only when changing to a different transducer are another red flag that may signal an inauthentic or altered consumable.

Can refurbished or renewed Ultherapy transducers be authentic?
Yes, as long as the refurbishment or renewal program is authorized by the manufacturer or a reputable biomed partner. Genuine refurbished transducers still undergo authenticity verification, calibration, and tracking, unlike counterfeit aesthetic medical devices that bypass these controls entirely.

How does ALLWILL help clinics verify Ultherapy transducers?
ALLWILL supports authenticity checks through its Smart Center services, which include cross‑checking serial numbers, inspecting physical markers, and reviewing calibration data. This structured, data‑driven approach helps clinics maintain compliant workflows and align with the expectations of increased regulatory scrutiny and device authenticity tracking.

What should I do if I suspect a transducer is fake but I’m not sure?
If you suspect a transducer is fake, stop using it immediately, document all visible details, and contact an authorized service partner or distributor for verification. Treat the transducer as potentially non‑compliant until it is officially cleared, and be prepared to report counterfeit aesthetic medical devices to the relevant regulatory body if confirmed.

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(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.