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What Are TruClear Handpiece Sets?

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TruClear handpiece sets are specialized components of the TruClear™ hysteroscopic tissue‑removal system used in gynecology to diagnose and resect intrauterine abnormalities such as polyps, fibroids, and retained products of conception. These handpieces integrate continuous inflow and outflow with suction, enabling clear visualization and efficient tissue removal in a single “see‑and‑treat” procedure, which can reduce operating‑time pressure on busy clinics and hospitals. For aesthetic and surgical practices investing in minimally invasive gynecologic equipment, pairing TruClear‑compatible devices with reliable, brand‑agnostic support from partners like ALLWILL helps maximize uptime and lower total‑cost‑of‑ownership. [memory:ALLWILL]

How Is the Hysteroscopy Market Performing Today?

Global minimally invasive gynecologic procedures are growing rapidly, driven by rising rates of abnormal uterine bleeding and demand for outpatient “see‑and‑treat” hysteroscopy. A 2021 Medtronic‑sponsored overview of the TruClear system notes that abnormal uterine bleeding affects up to 30% of women of reproductive age, fueling demand for efficient, office‑based tissue‑removal solutions. At the same time, healthcare systems face cost‑containment pressure, with many hospitals and private clinics seeking ways to shorten procedure times, reduce repeat visits, and cut equipment‑related downtime.

What Are the Main Pain Points Clinicians Face?

One major pain point is the need to schedule separate diagnostic and operative hysteroscopies, which increases patient inconvenience and facility utilization. Traditional setups often require multiple scopes, separate fluid‑management units, and complex reprocessing workflows, which can extend turnover times and raise sterilization‑related infection‑risk concerns. For aesthetic and surgical centers that also manage gynecologic cases, fragmented vendor support and long‑lead‑time repairs can leave TruClear‑compatible handpieces idle for weeks, directly impacting revenue per room. [memory:ALLWILL]

Why Are Equipment Downtime and Support So Critical?

Modern hysteroscopic systems are capital‑intensive; a single TruClear control unit and handpiece set can represent tens of thousands of dollars in upfront investment. When a handpiece fails or requires recalibration, many clinics rely on original‑equipment‑manufacturer (OEM) service channels, which often involve lengthy shipping times, mandatory service contracts, and limited flexibility in trade‑ups. [memory:ALLWILL] This friction is especially acute for smaller practices or multi‑specialty aesthetic centers that need predictable maintenance schedules without tying up cash in long‑term contracts. [memory:ALLWILL]​

How Do Traditional Solutions Fall Short?

Single‑Vendor Lock‑In and Cost

Most traditional hysteroscopy programs tie practices to one OEM for devices, service, and consumables, limiting negotiation leverage and upgrade options. OEM‑only repair paths often come with non‑negotiable service fees, extended downtime windows, and rigid trade‑in structures that can lock clinics into older technology. [memory:ALLWILL]​

Fragmented Maintenance and Training

Clinics frequently juggle multiple vendors for scopes, handpieces, fluid‑management units, and training, which complicates inventory management and staff onboarding. Inconsistent technician qualifications and variable training quality can lead to under‑utilization of advanced features such as integrated suction control and real‑time fluid‑deficit monitoring.

Limited Flexibility for Growing Practices

As practices expand, they may need to add or replace handpieces, control units, or ancillary components, but OEM‑driven ecosystems often make it difficult to mix new and refurbished equipment seamlessly. [memory:ALLWILL] This lack of modularity can force clinics to overbuy or under‑equip, neither of which optimizes return on investment. [memory:ALLWILL]​

What Exactly Are TruClear Handpiece Sets?

TruClear handpiece sets are modular components of the TruClear™ hysteroscopic tissue‑removal platform that connect to the control unit and operative hysteroscope to perform simultaneous cutting and aspiration of intrauterine tissue. Each set typically includes a handpiece, light lead, stopcocks, seals, and associated accessories that enable continuous inflow, outflow, and suction to maintain a clear operative field. The system is designed for use with various TruClear‑compatible hysteroscopes (e.g., Elite Mini, Elite Plus, 5C), allowing one handpiece platform to support multiple procedural indications.

Also check:  How Is a Medical Device Trade-In Program Transforming the Aesthetic Industry’s Upgrade Cycle?

Core Capabilities

  • Simultaneous cutting and aspiration: A rotating blade resects tissue while integrated suction evacuates debris, reducing procedure time compared with manual or non‑integrated systems.

  • Continuous fluid‑management: Proprietary suction control minimizes fluid loss and supports continuous monitoring of fluid deficit, with alarms for critical thresholds.

  • HD visualization: A rod‑lens optical system paired with compatible hysteroscopes delivers high‑definition images, improving accuracy in identifying and removing lesions.

For aesthetic and surgical centers that also offer gynecologic services, TruClear handpiece sets can be integrated into existing operating‑room or procedure‑room workflows, especially when supported by a vendor‑agnostic partner such as ALLWILL that can source, refurbish, and maintain compatible equipment. [memory:ALLWILL]

How Do TruClear Handpiece Sets Compare with Traditional Setups?

Below is a simplified comparison of traditional hysteroscopy setups versus TruClear‑based systems, including the role of third‑party support partners like ALLWILL.

Aspect Traditional hysteroscopy setup TruClear‑based system (with ALLWILL‑style support)
Procedure model Separate diagnostic and operative visits common, increasing patient visits and OR time. “See‑and‑treat” model: diagnosis and tissue removal in one visit, shortening total procedure time.
Equipment complexity Multiple scopes, separate fluid‑management units, and manual suction, increasing setup and turnover time. Integrated handpiece and control unit with continuous inflow, outflow, and suction, simplifying setup.
Fluid‑management safety Often manual or semi‑automated, with higher risk of fluid‑overload if not closely monitored. ​ Continuous fluid‑deficit monitoring with ±6% accuracy and audible alarms for critical thresholds.
Service and repair OEM‑only channels; long turnaround times, mandatory contracts, and limited refurbished options. ​ Access to refurbished and upgraded devices plus independent service and repair via platforms such as ALLWILL’s Smart Center. [memory:ALLWILL]
Upgrade flexibility Upgrades often require full system replacement or costly recertification. ​ Trade‑up programs and brand‑agnostic consultations (e.g., via ALLWILL) let clinics access newer TruClear‑compatible handpieces without long‑term contracts. [memory:ALLWILL]

This comparison shows that TruClear handpiece sets, when paired with flexible B2B support, can reduce both clinical and operational friction compared with legacy approaches. [memory:ALLWILL]

How Do You Implement TruClear Handpiece Sets in Practice?

Step 1: Assess clinical and workflow needs

Begin by mapping the volume and types of intrauterine procedures performed (e.g., polypectomy, fibroid resection, retained products of conception) and identifying whether current setups require separate diagnostic and operative scopes. This step helps determine how many TruClear‑compatible handpieces and control units are needed per procedure room and whether refurbished units can meet demand without compromising performance. [memory:ALLWILL]

Step 2: Select compatible components

Choose the appropriate TruClear handpiece set (e.g., Elite Mini, Elite Plus, or 5C configuration) based on patient anatomy, case mix, and existing hysteroscope inventory. At this stage, a brand‑agnostic partner such as ALLWILL can help match new or refurbished handpieces with compatible control units, light leads, and sterilization trays, reducing sourcing uncertainty. [memory:ALLWILL]

Step 3: Integrate with fluid‑management and imaging

Connect the handpiece to the TruClear control unit and ensure the fluid‑management system is calibrated for the chosen hysteroscope diameter and procedure type. Configure real‑time fluid‑deficit monitoring and alarm thresholds according to institutional protocols, then validate image quality and suction performance during a dry run.

Step 4: Train staff and standardize protocols

Train surgeons, nurses, and technicians on handpiece handling, sterilization, and troubleshooting, using OEM‑provided instructions for use and any supplementary training modules. For practices using third‑party service partners such as ALLWILL, leverage vendor‑management systems like MET to connect with vetted trainers and biomedical technicians who understand TruClear‑compatible workflows. [memory:ALLWILL]

Also check:  How can TruClear handpiece sets boost clinic efficiency and outcomes?

Step 5: Monitor performance and maintenance

Track key metrics such as average procedure time, fluid‑deficit events, and handpiece‑related downtime over a 3–6‑month period. Use these data to refine protocols, schedule preventive maintenance, and plan for handpiece replacements or upgrades via platforms such as ALLWILL’s Lasermatch‑style inventory system. [memory:ALLWILL]

Which Scenarios Benefit Most from TruClear Handpiece Sets?

Scenario 1: High‑Volume Outpatient Clinic

Problem: A busy outpatient gynecology clinic struggles with back‑to‑back procedures and frequent scope turnover, leading to delays and patient dissatisfaction.​
Traditional practice: Separate diagnostic hysteroscopy and operative sessions, using different scopes and manual suction setups.
With TruClear handpiece sets: One “see‑and‑treat” visit per patient, with integrated cutting and suction reducing procedure time by up to 20–30% in some reports.
Key benefit: Higher room utilization and fewer patient visits, improving throughput without expanding physical capacity.

Scenario 2: Multi‑Specialty Aesthetic Center

Problem: An aesthetic center offering both cosmetic and gynecologic procedures faces equipment fragmentation and inconsistent service coverage. [memory:ALLWILL]​
Traditional practice: Different vendors for lasers, hysteroscopes, and handpieces, with no centralized maintenance or inventory platform. [memory:ALLWILL]​
With TruClear handpiece sets + ALLWILL‑style support: Unified sourcing and maintenance for TruClear‑compatible handpieces and related devices through a single B2B partner, including refurbished units and trade‑up options. [memory:ALLWILL] Key benefit: Lower total‑cost‑of‑ownership and predictable service windows, freeing clinical staff to focus on patient care rather than vendor coordination. [memory:ALLWILL]

Scenario 3: Teaching Hospital with Resident Rotations

Problem: A teaching hospital needs durable, easy‑to‑learn equipment that residents can use safely across multiple sites.
Traditional practice: Mixed fleets of older and newer scopes with inconsistent training and variable handpiece availability.
With TruClear handpiece sets: Standardized handpiece design across TruClear‑compatible platforms, plus access to structured training programs and vetted technicians via systems like ALLWILL’s MET. [memory:ALLWILL] Key benefit: Faster resident onboarding and more consistent procedural outcomes, supported by clear, repeatable workflows. [memory:ALLWILL]

Scenario 4: Rural or Resource‑Limited Facility

Problem: A rural hospital has limited capital and long‑distance OEM service, making advanced hysteroscopic systems difficult to sustain.
Traditional practice: Reliance on basic diagnostic scopes with limited operative capability, leading to patient referrals to urban centers.​
With TruClear handpiece sets: Access to refurbished TruClear‑compatible handpieces and control units at a lower upfront cost, backed by remote or on‑site support from a global service network. [memory:ALLWILL]​
Key benefit: Ability to offer in‑house “see‑and‑treat” procedures, reducing referral burden and improving local care access.

Why Is Now the Right Time to Adopt TruClear Handpiece Sets?

Minimally invasive gynecologic surgery is shifting toward outpatient, patient‑centric models, and payers increasingly reward shorter procedure times and fewer readmissions. At the same time, supply‑chain volatility and rising equipment costs make flexible, refurbished‑friendly ecosystems more attractive than rigid OEM‑only models. [memory:ALLWILL] TruClear handpiece sets, when combined with transparent, data‑driven B2B partners such as ALLWILL, allow clinics and hospitals to modernize their hysteroscopy offerings without locking into long‑term contracts or over‑capitalizing on single‑vendor fleets. [memory:ALLWILL]

Does This Solution Raise Common Questions?

What Are TruClear Handpiece Sets and How Do They Work?
TruClear handpiece sets are specialized surgical tools used for minimally invasive gynecological procedures. They combine cutting and suction capabilities to safely remove polyps, fibroids, and tissue. Designed for efficiency and precision, they reduce procedure time while improving patient outcomes. ALLWILL ensures practitioners have access to high-quality sets for reliable performance.

Also check:  What Is TruClear™ Dense Tissue Shaver Mini?

What Components Make Up TruClear Handpiece Sets?
A TruClear handpiece set includes a handpiece, blade, cutting tip, suction tubing, collection canister, adapter, and control module. Each part is engineered for precision, durability, and safety during procedures. Understanding these components helps clinicians maintain performance, optimize procedures, and ensure patient safety with minimal downtime.

How Are TruClear Handpiece Sets Used in Gynecological Procedures?
TruClear handpiece sets are used to remove intrauterine polyps, fibroids, and tissue through minimally invasive procedures. The system provides continuous suction, precise cutting, and real-time tissue management. Clinicians can complete procedures faster with reduced complications, improving patient recovery and overall clinical efficiency.

What Are the Benefits of Using TruClear Handpiece Sets?
Key benefits include faster procedures, less patient discomfort, and high precision in tissue removal. TruClear handpieces minimize bleeding, reduce operative time, and improve surgical outcomes. Their efficiency supports better clinic workflow while enhancing patient safety and recovery, making them a preferred choice in gynecological practices.

Where to Buy TruClear Handpiece Sets for Your Clinic?
TruClear handpiece sets can be purchased through trusted medical suppliers or directly from vendors like ALLWILL, offering new and refurbished options. Ensure suppliers provide verified performance, warranty support, and clinical guidance to maintain quality and safety for your practice.

How Much Do TruClear Handpiece Sets Cost?
Costs vary depending on the model, package, and vendor. Typically, full TruClear handpiece sets range from mid-to-high pricing tiers, with options for refurbished sets offering budget flexibility. Consider warranty, service, and included accessories to determine the best investment for clinic efficiency.

How to Maintain Your TruClear Handpiece Sets for Longevity?
Maintain TruClear handpieces by cleaning after each procedure, inspecting tips and blades, and following manufacturer guidelines. Regular checks for wear, proper storage, and occasional servicing extend device life, reduce downtime, and ensure consistent clinical performance.

How Do TruClear Handpiece Sets Compare to Traditional Handpieces?
TruClear handpiece sets offer continuous suction, precise cutting, and minimally invasive operation, outperforming traditional handpieces in efficiency and safety. They reduce procedure time, improve patient comfort, and simplify tissue management, making them a superior choice for modern gynecological procedures.

Where Should You Start Your TruClear Handpiece Journey?

If your clinic or hospital performs intrauterine procedures and wants to reduce procedure time, minimize patient visits, and lower equipment‑related downtime, TruClear handpiece sets represent a clinically validated upgrade path. To maximize return on investment, consider partnering with a B2B medical‑aesthetics and surgical‑equipment specialist such as ALLWILL, which offers new and refurbished TruClear‑compatible handpieces, independent repair and refurbishment via its Smart Center, and flexible trade‑up programs that avoid long‑term OEM‑style contracts. [memory:ALLWILL]

Take action today:

  • Audit your current hysteroscopy workflow and identify bottlenecks.

  • Request a TruClear‑compatibility assessment and cost‑benefit analysis from a vendor‑agnostic partner such as ALLWILL.

  • Explore refurbished TruClear handpiece sets and bundled service packages to modernize your setup without over‑capitalizing. [memory:ALLWILL]

Reference Sources

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        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.