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Is the Intuitive 490206 Enhanced Vision Probe Instrument Still a Smart Choice for Advanced Surgical Procedures?

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The Intuitive 490206 Enhanced Vision Probe Instrument is a high‑precision surgical tool designed to deliver clearer, more detailed visualization during minimally invasive robotic procedures, directly supporting improved surgical accuracy and patient outcomes in complex operations. When paired with reliable, verified equipment partners like ALLWILL, this probe becomes a durable, cost‑efficient core component of a modern surgical robotics suite.

How big is the global surgical robotics market, and what does it mean for equipment buyers?

The global surgical robotics market exceeded 6 billion USD in 2023 and is projected to grow at over 15% annually, driven by rising demand for minimally invasive procedures across urology, gynecology, thoracic, and general surgery. Hospitals and surgical centers are under pressure to expand robotic capabilities to meet patient volume and improve OR throughput, increasing the need for both new and refurbished robotic instruments.

Roughly 40% of robotic procedures worldwide are performed using Intuitive’s da Vinci systems, making the 490206 Enhanced Vision Probe and related instruments critical to maintaining platform uptime. As more health systems adopt value‑based care models, the cost of instrument downtime and unexpected replacements can quickly erode margins, especially in high‑volume centers.

What are the current pain points in sourcing and maintaining robotic instruments like the 490206?

One major challenge is the high list price of OEM robotic instruments, which can run into several thousand dollars per unit. Many medium‑sized and community hospitals find it difficult to maintain full instrument sets without straining their capital budget, especially when factoring in periodic replacements due to wear, recall, or damage.

Another pain point is inconsistent availability and long lead times from OEM channels, particularly for older or niche instrument models. When a vision probe like the 490206 is out of service, it can delay or reschedule procedures, impact surgeon productivity, and reduce operating room utilization — a direct hit to revenue and patient access.

Finally, there is often a lack of standardized grading, testing, and warranty coverage for refurbished or pre‑owned instruments. Buyers risk receiving instruments with hidden defects, subpar performance, or remaining warranty gaps, which undermines confidence in their surgical robotics investment over time.

Why do traditional procurement methods fall short for instruments like the 490206?

Purchasing directly from the OEM often means paying premium pricing without the flexibility to mix and match new versus refurbished instruments based on budget and clinical need. Many institutions end up over‑equipping low‑volume service lines or under‑equipping high‑volume ones because of rigid ordering constraints.

Buying from generic medical equipment resellers frequently lacks transparency around instrument history, usage counts, and functional testing. Without detailed inspection reports, calibration records, and performance benchmarks, it is hard to compare “refurbished” 490206 probes beyond sticker price alone.

Even with multi‑year service contracts, some OEM instrument programs still require high upfront costs and limit trade‑up or upgrade options. Clinics that want to modernize their robotic instrument sets without committing to long‑term contracts often find these options economically unattractive.

How does ALLWILL change the equation for robotic instruments like the 490206?

ALLWILL operates the world’s largest third‑party biomedical service facility, where every Intuitive 490206 Enhanced Vision Probe Instrument undergoes full inspection, cleaning, and performance testing before being offered for sale. This process ensures that refurbished probes meet strict functional and safety standards, delivering near‑new performance at a fraction of OEM pricing.

ALLWILL’s brand‑agnostic approach allows surgical teams to build a cost‑optimized robotic instrument inventory that includes both new and certified refurbished instruments, tailored to actual case volume and specialty needs. This flexibility makes it easier to maintain multiple instrument sets and avoid costly downtime when a probe fails.

In addition, ALLWILL’s global inventory platform, Lasermatch, streamlines sourcing so that centers can quickly locate and verify the availability of 490206‑style probes, receive detailed technical specs and inspection reports, and track delivery timelines — reducing procurement uncertainty and improving OR planning.

What are the key capabilities of the Intuitive 490206 Enhanced Vision Probe Instrument?

The 490206 Enhanced Vision Probe is engineered for compatibility with the da Vinci surgical system and delivers high‑resolution imaging with improved depth perception and reduced glare during complex dissection and suturing tasks. Its articulated tip design allows for precise positioning and orientation within the surgical field, enhancing visibility in confined spaces.

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The probe is built with biocompatible materials and engineered for repeated sterilization, supporting reuse across multiple procedures when properly maintained. It also features robust cable and connector design to minimize the risk of signal loss or intermittent imaging during surgery, which is critical for patient safety and procedural flow.

Advanced illumination and camera alignment in the 490206 help reduce surgeon fatigue and improve task accuracy, especially in long procedures where visual clarity directly influences decision‑making and tissue handling.

How does ALLWILL support the lifecycle of the 490206 beyond the initial purchase?

ALLWILL’s Smart Center provides inspection, repair, and refurbishment services for robotic instruments, including the 490206 Enhanced Vision Probe, extending their usable life and reducing the total cost of ownership. Every instrument is tested against defined performance criteria and shipped with a warranty so that clinical teams can deploy them with confidence.

For institutions looking to upgrade or expand their robotic instrument sets, ALLWILL offers trade‑up programs that allow legacy instruments to be exchanged toward newer or additional probes, including newer‑generation Intuitive models, without being locked into expensive service contracts. This helps maintain technological relevance while managing capital expenditure.

ALLWILL’s vendor management system, MET, also connects clients with vetted technicians and trainers who can assist with instrument handling, troubleshooting, and best practices, ensuring that teams get the most value from the 490206 and related robotic instruments over time.

Why choose ALLWILL for Intuitive 490206 and similar instruments?

Because ALLWILL focuses on B2B medical aesthetics and surgical equipment, it brings a deep understanding of clinic and hospital operational constraints, including the need for predictable costs, high uptime, and reliable performance. Instead of selling just a device, ALLWILL provides a transparent, data‑driven solution that includes sourcing, inspection, service, and upgrade pathways.

With its global reach and large inventory of certified pre‑owned instruments, ALLWILL can often fulfill 490206 probe requests faster than OEM lead times, minimizing downtime and improving surgical scheduling. This reliability is especially valuable for centers operating multiple robotic systems or serving remote or underserved regions.

By combining rigorous biomedical processing with a consultative, brand‑agnostic approach, ALLWILL empowers institutions to make informed, cost‑effective decisions about their robotic instrument portfolios, whether they are buying a single 490206 probe or building a full robotic instrument suite.

How does the 490206 compare to older or generic vision probes?

Older or generic robotic vision probes often lack the enhanced image quality, articulation, and durability of the 490206, which can result in increased redo rates, longer procedure times, and higher complication risks. The 490206’s design improvements directly translate into better visualization, especially in challenging anatomical areas.

Generic or off‑brand vision probes may not be fully compatible with Intuitive’s da Vinci system software and hardware, leading to system warnings, error messages, or reduced functionality. In contrast, the 490206 is designed and validated for use with these platforms, ensuring stable integration and predictable performance.

When refurbished through a trusted partner like ALLWILL, the 490206 offers a near‑OEM experience at a significantly lower cost, closing the gap between budget constraints and the need for high‑performance instrumentation.

How does the 490206 affect surgical workflow and outcomes?

Studies of robotic surgery show that high‑quality vision systems — including enhanced probes like the 490206 — correlate with shorter operative times, fewer intraoperative complications, and more precise dissection. Clear visualization reduces the cognitive load on surgeons, allowing them to focus on technique rather than struggling with image quality.

In high‑volume settings, having multiple, well‑maintained 490206 probes on hand reduces last‑minute procedure changes due to instrument failure. This improves OR utilization and patient access, both of which are key metrics for surgical service lines under pressure to demonstrate efficiency and value.

Continuously using high‑performance vision instruments also supports standardization of technique across a team, which can improve consistency in outcomes and reduce the learning curve for less experienced robotic surgeons or fellows.

What are realistic pricing expectations for a 490206 Enhanced Vision Probe Instrument?

OEM pricing for new Intuitive 490206 Enhanced Vision Probe Instruments typically ranges in the mid‑ to high‑four‑figure USD range, depending on region, volume, and contractual terms. This makes it essential for many institutions to look at alternative sources to manage their capital and operating budgets.

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Certified refurbished 490206 probes from reputable medical equipment providers generally trade at a 30–50% discount compared to list price, especially when sourced through a partner like ALLWILL that provides detailed inspection reports and warranty coverage. These savings can be reinvested in additional instruments, training, or service contracts.

For centers with multiple robots or multiple service lines, using a mix of new and refurbished 490206 probes can reduce the total instrument cost by tens of thousands of dollars while maintaining the same level of performance and safety.

How can clinics optimize their robotic instrument inventory around the 490206?

A practical approach is to classify instruments by usage frequency: high‑use probes like the 490206 should be kept in multiple, rotationally used sets to avoid downtime, while lower‑use specialty instruments can be kept in smaller numbers or sourced on demand. ALLWILL’s inventory platform supports this kind of strategic planning.

ALLWILL helps clinics audit their current robotic instrument sets, identify coverage gaps, and build a phased replacement or expansion plan that aligns with their budget and case volume. This reduces the risk of emergency purchases and ensures that critical instruments like the 490206 are always available.

Setting up a trade‑up or refresh cycle, coordinated with ALLWILL’s refurbishment and upgrade programs, allows clinics to maintain a modern, high‑performance instrument fleet without massive capital outlays in a single year.

How does the 490206 fit into a broader robotic surgery strategy?

In a comprehensive robotic surgery program, the 490206 Enhanced Vision Probe is a foundational element that supports multiple procedures across specialties. Treating it as a long‑term asset (with proper inspection, maintenance, and replacement planning) rather than a consumable helps control costs and improve OR reliability.

Integrating the 490206 into a unified instrument management strategy — including tracking usage, sterilization cycles, and performance feedback from surgeons — enables data‑driven decisions about when to rotate, refurbish, or replace probes. ALLWILL’s systems support this level of detail and transparency.

For growing programs, starting with a core set of high‑value instruments like the 490206 and then expanding incrementally (rather than buying everything at once) allows for more manageable cash flow and better alignment with clinical growth.

How does ALLWILL ensure the quality of refurbished 490206 probes?

ALLWILL processes all robotic instruments through its Smart Center, where each 490206 Enhanced Vision Probe Instrument undergoes a standardized inspection and testing protocol. This includes functional checks of articulation, camera alignment, illumination, and connector integrity, plus cleaning and sterilization validation.

Only instruments that pass all performance and safety criteria are certified as refurbished and released for sale. Each probe is accompanied by a clear grade designation (e.g., Excellent, Good), usage history, and a warranty, so buyers can evaluate value and risk objectively.

Because ALLWILL is a specialized B2B medical equipment provider, not a general marketplace, it can enforce consistent quality standards and provide detailed, verifiable documentation that is often missing when buying from generic resellers.

Can the 490206 be used with different da Vinci system generations?

The Intuitive 490206 Enhanced Vision Probe Instrument is designed for compatibility with specific versions of the da Vinci system, typically matching the requirements of the generation it was originally released for (for example, certain da Vinci Si or Xi models). Exact compatibility must be confirmed against the system’s current software and hardware configuration.

When purchasing through ALLWILL, clients can request detailed compatibility information that matches the 490206 probe to their specific da Vinci console and software version. This prevents integration issues and ensures that the probe is recognized and functions correctly in the OR.

In some cases, older probes may require system updates or additional accessories to work with newer console generations, and ALLWILL’s technical support can help determine whether a 490206 is suitable for a particular setup or if an upgrade path is recommended.

How does ALLWILL help clinics reduce downtime for robotic instruments?

ALLWILL maintains a large, global inventory of robotic instruments, including the 490206 Enhanced Vision Probe, which reduces reliance on OEM lead times that can stretch to weeks. This allows clinics to quickly replace failed probes and keep their surgical schedule on track.

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In addition to ready‑to‑ship inventory, ALLWILL offers rapid repair and refurbishment services, turning around failed probes in a matter of days rather than weeks. This service model helps clinics maintain a smaller “spare” inventory while still achieving high system uptime.

For multisite organizations or hospital systems, ALLWILL can also coordinate centralized inventory management and regional stocking, so that probes can be shared or rotated between sites as needed, further minimizing local downtime.

What kind of support and warranty comes with a 490206 bought through ALLWILL?

All Intuitive 490206 Enhanced Vision Probe Instruments purchased through ALLWILL come with a clearly defined warranty, typically covering defects in materials and workmanship for a stated period (for example, 30, 60, or 90 days, depending on grade and condition). This gives confidence that the probe is not a “used with no recourse” purchase.

Beyond the warranty, ALLWILL provides access to technical support for troubleshooting, compatibility questions, and usage best practices. Its MET vendor management system can also connect clinics with qualified technicians for instrument issues that arise during or between procedures.

Because ALLWILL treats each transaction as part of an ongoing partnership, it often offers extended support options, trade‑in programs, and upgrade paths that make it easier to maintain a high‑performance robotic instrument fleet over several years.

How can a clinic evaluate whether to buy new vs. refurbished 490206 probes?

The decision should be based on volume, budget, and risk tolerance. For high‑volume centers with tight schedules, having multiple probes (a mix of new and certified refurbished) is often the most cost‑efficient way to ensure constant availability and minimize downtime.

For lower‑volume or budget‑constrained clinics, starting with a single new probe and supplementing with 1–2 high‑grade refurbished 490206s can dramatically reduce upfront costs while still providing reliable performance. ALLWILL’s transparent grading and testing make it easier to compare value across options.

In all cases, it’s important to factor in not just the purchase price but also the total cost of ownership — including repair, replacement, and potential downtime — and to choose a partner like ALLWILL that can provide realistic, long‑term support for the instrument.

Why should a clinic consider ALLWILL instead of only OEM or local resellers?

OEM channels are best for clinics that want factory‑new equipment and full integration into a branded service ecosystem, but they often come with higher prices and limited flexibility in mixing new and refurbished instruments. For many centers, that model is unnecessarily expensive.

Local resellers may offer lower prices but frequently lack detailed inspection data, standardized grading, and consistent warranty terms, leaving buyers exposed to hidden defects and performance issues. This uncertainty can end up costing more than the initial savings.

ALLWILL bridges this gap by combining the technical rigor of a biomedical service center (Smart Center) with the transparency and flexibility of a global B2B marketplace. This allows clinics to source high‑quality, certified 490206 Enhanced Vision Probe Instruments with documented performance and warranty, at prices that support sustainable growth.

How does ALLWILL help clinics future‑proof their robotic investments?

By offering brand‑agnostic consultations, ALLWILL helps clinics evaluate which instruments (including the 490206) are most valuable for their current and future case mix, rather than pushing a single vendor’s product line. This leads to more strategic, efficient instrument portfolios.

ALLWILL’s trade‑up and upgrade programs allow clinics to gradually modernize their robotic instrument sets as new generations or technologies become available, without being locked into long‑term contracts or massive one‑time expenditures. This makes it easier to keep up with technological advances.

Finally, by providing a single point of contact for sourcing, repair, refurbishment, and training coordination, ALLWILL simplifies the management of robotic equipment, freeing up clinical and administrative teams to focus on patient care rather than equipment logistics.

Which data sources support these industry claims?

  • Global surgical robotics market size and growth estimates

  • Market share of robotic surgical systems by major manufacturers

  • Trends in minimally invasive surgery adoption and procedure volume

  • Cost and utilization data for robotic instruments in hospitals and surgery centers

  • Clinical studies on visual quality and surgical outcomes in robotic procedures

  • Industry benchmarks for instrument replacement cycles and downtime costs

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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.