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Intuitive 490206 Enhanced Vision Probe Instrument for Advanced Robotic Procedures

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The Intuitive 490206 Enhanced Vision Probe Instrument is a next‑generation peripheral vision probe designed for the Ion endoluminal system and advanced minimally invasive procedures in the lung. As interventional pulmonology, robotic bronchoscopy, and precision oncology evolve, many hospitals are asking whether this enhanced vision probe is still a smart choice for complex cases, high‑risk patients, and long‑term capital planning.

What Is the Intuitive 490206 Enhanced Vision Probe Instrument?

The Intuitive 490206 Enhanced Vision Probe Instrument is an upgraded peripheral vision probe engineered for use with the Ion endoluminal robotic platform. It is a slim, videoscopic probe that fits inside the Ion fully articulating catheter to provide direct visualization of the bronchial tree and peripheral airways during navigation and biopsy.

Unlike conventional bronchoscopes or earlier peripheral vision probes, the 490206 model is optimized for high‑definition imaging, a wider field of view, and smoother insertion and removal. It is specifically compatible with Ion systems running version 1.45 or higher and P3 software or later, ensuring that its optical and usability improvements can be fully leveraged in modern robotic bronchoscopy suites.

Core Design and Field-of-View Advantages of the 490206 Vision Probe

A key selling point of the Intuitive 490206 Enhanced Vision Probe Instrument is its wider field of view compared with the previous Ion peripheral vision probe. The earlier 490106 probe provided a 90‑degree field of view, which already represented a significant step forward versus standard bronchoscopes. The enhanced 490206 probe expands this to approximately a 120‑degree field of view, offering a noticeably broader visual envelope for navigation and anatomy identification.

This wider field of view helps interventional pulmonologists see more of the airway wall, bifurcations, and subtle anatomical landmarks without constant camera reorientation. In practical terms, it reduces blind spots when steering through subsegmental bronchi toward small peripheral nodules. When combined with Ion’s fiber‑optic shape sensing and virtual navigation, this enhanced visualization can translate into greater confidence that the catheter and biopsy needle are tracking along the intended path.

Another core improvement is image sharpness. Internal testing from Intuitive indicates up to twice the image quality compared with the prior probe, with sharper videoscopic rendering of mucosal patterns and airway structures. In the context of advanced robotic bronchoscopy, that higher image quality supports more precise confirmation of location, especially when cross‑checking with fluoroscopy, radial EBUS, or 3D imaging such as CBCT.

Compatibility, Workflow, and System Integration

The Intuitive 490206 Enhanced Vision Probe Instrument is designed for seamless integration into the Ion endoluminal workflow. It slides through the 2 mm working channel of the Ion fully articulating catheter, which itself has an outer diameter of about 3.5 mm. This combination allows access deep into peripheral lung segments while maintaining enough internal space for ancillary tools and suction adapters.

The probe’s design supports quick installation and removal, which matters during complex cases where clinicians alternate between vision, radial EBUS probes, biopsy needles, and other third‑party tools. The smooth ergonomics reduce fiddling at the table and enable the bronchoscopist to focus on target access, lesion confirmation, and tool‑in‑lesion verification.

Because the 490206 probe is only supported on Ion systems at or above version 1.45 with P3 software, it effectively encourages institutions to maintain up‑to‑date firmware and software. That alignment ensures that the enhanced vision probe can participate fully in advanced features such as synchronized live and virtual views, integrated 3D imaging, and improved navigation algorithms.

Clinical Use Cases: Peripheral Lung Nodules and Complex Airway Access

The strongest clinical use case for the Intuitive 490206 Enhanced Vision Probe Instrument is robotic‑assisted bronchoscopy for small, peripheral pulmonary nodules. Many lung lesions detected on screening CT scans reside in distal segments or subsegments, where conventional flexible bronchoscopes struggle to reach reliably without significant scope looping or loss of positional control.

With Ion’s ultra‑thin, highly maneuverable catheter and real‑time shape sensing, the enhanced vision probe allows clinicians to see within narrow airways while the robotic system continuously tracks the three‑dimensional shape of the catheter. This combination is particularly useful when making tight turns in upper lobe segments or navigating tortuous paths in emphysematous lungs.

Beyond nodules, the 490206 probe can support sampling in cases involving suspected metastatic lesions, inflammatory nodules, or lesions adjacent to, but not directly within, visible airway lumens. The wide field of view helps operators orient themselves relative to branching patterns, which is critical when moving from segmental to subsegmental levels. It also supports safer navigation near major vessels and fissures by improving spatial awareness inside the bronchial tree.

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Market Trends and Demand for Enhanced Vision Robotic Bronchoscopy

Market data from major medical device reports shows that robotic bronchoscopy and advanced imaging for peripheral lung lesions have grown substantially due to global lung cancer screening initiatives and earlier CT‑based detection. As low‑dose CT screening becomes standard, more small nodules are identified at earlier stages, driving demand for precise, minimally invasive biopsy options.

Within this landscape, the Intuitive Ion system and its associated instruments occupy a premium segment. Hospitals are increasingly evaluating robotic bronchoscopy platforms based on navigation precision, lesion localization accuracy, and the ability to integrate multi‑modal imaging. Enhanced vision probes with wider fields of view and sharper optical performance are becoming baseline expectations rather than optional upgrades.

The Intuitive 490206 Enhanced Vision Probe Instrument sits directly in this trend. It reinforces the Ion platform’s value proposition by improving the clarity and scope of the visual information that underpins each navigation decision. As more outcomes data accumulates around tool‑in‑lesion accuracy, diagnostic yield, and complication rates for robotic bronchoscopy systems, visual performance of the vision probe becomes a critical differentiator.

Company Background: ALLWILL and Strategic Sourcing of Advanced Instruments

Advanced instruments like the Intuitive 490206 Enhanced Vision Probe Instrument often require careful sourcing, lifecycle management, and integration into existing fleets of robotic platforms. ALLWILL is redefining B2B medical aesthetics and broader medical technology sourcing by emphasizing innovation, trust, and operational efficiency for practitioners facing complex equipment decisions.

By combining a Smart Center for device inspection and refurbishment, a vendor management system that connects providers with vetted technicians, and an inventory platform that streamlines acquisition, ALLWILL helps clinicians and administrators optimize their capital investments. This type of support can be especially valuable when adding or upgrading specialized robotic accessories such as the 490206 enhanced vision probe, which must consistently meet high performance standards while fitting within tight budgetary and service constraints.

Technology Overview: How the Ion Vision Probe Works

The Ion system uses a fully articulating catheter with an embedded fiber‑optic shape sensor to determine catheter shape hundreds of times per second. The Intuitive 490206 Enhanced Vision Probe Instrument is threaded through the catheter’s working channel, providing direct videoscopic visualization of the airways as the system calculates real‑time position and heading.

The vision probe’s camera generates a 120‑degree field of view image, which can be displayed alongside a virtual map derived from pre‑procedural CT scans. Clinicians can watch a synchronized representation of their location in the CT‑based model and the live camera view simultaneously, effectively overlaying anatomical reality with a digital roadmap.

The enhanced resolution of the 490206 probe supports better visual discrimination of small luminal variations, airway wall irregularities, and subtle anatomic cues such as secondary carinae. When combined with fluoroscopy, radial EBUS, and in some configurations integrated 3D imaging from systems like Cios Spin, it contributes to a multi‑layered navigation environment that is far more informative than a single imaging modality alone.

Comparison: 490206 Enhanced Vision Probe vs 490106 Peripheral Vision Probe

To determine whether the 490206 enhanced version is still a smart choice, it is critical to compare it with the prior Ion peripheral vision probe and evaluate how the upgrades impact clinical practice and ROI.

Probe Model Field of View Image Quality System Compatibility Key Advantages Typical Use Cases
490106 Ion Peripheral Vision Probe Approximately 90 degrees Baseline HD Ion systems – earlier software versions supported Adequate visualization for early Ion adopters, supports direct airway visualization during navigation Standard robotic bronchoscopy for accessible peripheral nodules
490206 Enhanced Vision Probe Instrument Approximately 120 degrees Sharper, up to 2x improved image quality compared with prior probe Ion systems 1.45 or higher with P3 software or later Wider field of view, improved anatomy identification, easier installation and removal, enhanced user experience Complex peripheral nodules, challenging segmental access, cases requiring high confidence in tool‑in‑lesion alignment

The shift from 90 to 120 degrees of coverage increases the visible sector in front of the probe, which translates into fewer camera adjustments and more continuous contextual awareness. Also, the usability enhancements reduce friction during insertion and withdrawal, which can be particularly important when multiple instrument exchanges occur in a single case.

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Competitor Comparison: Intuitive 490206 Vision Probe vs Other Robotic Bronchoscopy Solutions

Robotic bronchoscopy is a competitive arena that includes multiple platforms with different vision and navigation philosophies. While naming specific brands is less important than evaluating features, the comparison typically centers on field of view, image clarity, navigation accuracy, and ecosystem integration.

System Component Intuitive 490206 with Ion Alternative Robotic Bronchoscopy Vision Solutions Key Takeaway
Primary Imaging Modality Peripheral videoscopic vision probe with wide field of view and HD imaging Varies: integrated bronchoscopic imaging, external scopes, or proprietary cameras Enhanced field and sharpness support precise navigation and anatomy identification in small airways
Navigation Backbone Fiber‑optic shape sensing, virtual CT‑based roadmaps, multi‑modal image synchronization Electromagnetic navigation, robotic guidance, or hybrid systems Shape sensing combined with wide‑angle vision can improve stability and positional confidence
Imaging Integration Designed to align with fluoroscopy, radial EBUS, and optional 3D imaging May integrate selectively depending on vendor A cohesive ecosystem reduces workflow fragmentation and aids accurate targeting
Upgradability Requires modern Ion software and hardware versions, enabling continuous feature additions Upgrade paths vary by platform The 490206 probe benefits from ongoing software improvements, which can extend life and ROI
Typical Clinical Focus Early‑stage lung cancer nodules, small peripheral lesions, precision biopsies Similar focus, sometimes broader airway interventions The enhanced vision probe is well positioned in the core high‑value use case of peripheral nodule biopsy

Against this competitive backdrop, the Intuitive 490206 Enhanced Vision Probe Instrument retains a strong value proposition by emphasizing visualization quality, integration, and a stable, well‑supported ecosystem.

Real-World Clinical Benefits and Potential ROI

Real‑world ROI for a device like the 490206 vision probe can be divided into clinical outcomes, workflow efficiency, and financial impact. Clinically, improved visualization and navigation are associated with higher tool‑in‑lesion rates and potentially higher diagnostic yield. When a higher percentage of bronchoscopic biopsy attempts successfully obtain diagnostic tissue, fewer patients require repeat invasive procedures such as CT‑guided transthoracic biopsy or surgical wedge resection.

From a workflow perspective, the easier installation and wider field of view reduce the time spent wrestling with limited visualization or suboptimal angles. The ability to maintain a clear and stable view as the catheter advances allows operators to perform more efficient passes, and potentially reduces the overall procedure length. Over time, this can translate into higher throughput in the bronchoscopy suite and less sedation time per patient.

Financially, a higher diagnostic yield and reduced reliance on additional procedures contribute to more efficient resource utilization. Institutions can justify the up‑front cost of the enhanced vision probe as part of a broader Ion system investment, particularly if the procedure volume for peripheral lung nodules is substantial. In some markets, being able to offer cutting‑edge robotic bronchoscopy with a proven enhanced vision probe also strengthens an institution’s competitive standing, attracting referrals from community hospitals and screening programs.

Safety, Learning Curve, and User Experience

Any advanced instrument must be evaluated not just on technical performance but also on safety and ease of adoption. The Intuitive 490206 Enhanced Vision Probe Instrument is designed with ergonomics and user‑friendly insertion in mind, leveraging a form factor that bronchoscopists already recognize. The user interface is integrated into Ion’s workflow, so the visual output and navigation aids are presented in a consistent, intuitive layout.

The learning curve for clinicians who already use Ion with the older probe is minimal. Transitioning to the enhanced probe primarily involves appreciating the wider field of view and sharper image, not relearning instrument handling. For new robotic bronchoscopy programs, the combination of real‑time shape sensing, virtual navigation, and high‑quality vision can actually simplify the learning path compared with more fragmented or less integrated solutions.

Safety benefits from clear visualization, stable catheter positioning, and compatibility with adjunctive imaging. The more accurately operators can see and understand airway anatomy, the better they can avoid unintended trauma, minimize bleeding, and steer clear of dangerous vascular structures. The 490206 probe’s visual clarity and broad view directly support these safety goals.

Future-Proofing: How Long Will the 490206 Stay Relevant?

A critical question for capital equipment planning is whether the Intuitive 490206 Enhanced Vision Probe Instrument will remain relevant as robotic platforms and imaging standards evolve. Several factors suggest that its utility will extend over the medium to long term.

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First, the 490206 probe is already aligned with newer Ion software versions, positioning it as the current optical standard within the Ion ecosystem. As additional software features roll out, such as enhanced image processing, AI‑assisted navigation, or improved CT‑to‑body divergence compensation, the wide‑angle, high‑resolution video feed from the 490206 probe will remain a critical input.

Second, the core clinical problem it addresses—accurate, minimally invasive biopsy of small peripheral lung nodules—is not going away. If anything, ongoing expansion of lung cancer screening will increase the number of patients requiring precise bronchoscopy. A vision probe that can reach deep into the lung and deliver clear, wide‑angle imaging will continue to be central to that workflow.

Finally, the probe’s dependence on software and firmware upgrades provides a natural pathway for enhancement over time. Even if the optical hardware remains largely consistent, the way the system processes, displays, and combines that visual data with other imaging modalities can continue to improve, effectively extending the working life and relevance of the 490206 instrument.

Is the Intuitive 490206 Enhanced Vision Probe Instrument Still a Smart Choice?

Evaluated against current market expectations, technological benchmarks, and clinical needs, the Intuitive 490206 Enhanced Vision Probe Instrument clearly remains a smart choice for advanced surgical and interventional procedures in the lung. It delivers a wider field of view than its predecessor, sharper video quality for anatomy identification, and improved ergonomics that enhance user experience in the Ion endoluminal system.

For institutions that already operate Ion platforms or are planning to implement robotic bronchoscopy for peripheral lung nodules, the 490206 probe is effectively the standard that aligns with modern navigation and imaging capabilities. Its integration with shape sensing, synchronized CT‑based virtual maps, and multi‑modal imaging means that it is not just an optical accessory but a core element of a sophisticated robotic ecosystem.

In an environment where precision, safety, diagnostic yield, and patient experience drive purchasing decisions, the 490206 enhanced vision probe is strongly positioned. For many hospitals and interventional pulmonology programs, investing in or maintaining the Intuitive 490206 Enhanced Vision Probe Instrument is still a strategically sound decision for delivering high‑level, minimally invasive care.

Practical Considerations Before Investing

Before committing to or expanding an inventory of the Intuitive 490206 Enhanced Vision Probe Instrument, decision‑makers should examine a few practical factors. Existing Ion system versions, software levels, and integration with imaging technologies should be audited to ensure full compatibility. Procedure volume for peripheral lung nodules and anticipated growth from screening programs should be projected to model potential ROI.

Service support, training capacity, and inventory management also matter. Ensuring that local teams are fully trained on both the Ion platform and the enhanced vision probe, that spare units are available, and that maintenance pathways are clearly defined will protect uptime. Partnering with organizations that specialize in managing advanced devices—whether internal teams or external partners—can further optimize the ownership experience.

For programs that prioritize cutting‑edge interventional pulmonary care, the Intuitive 490206 Enhanced Vision Probe Instrument continues to be a highly relevant, high‑value component of an advanced robotic bronchoscopy strategy, combining enhanced visualization, robust system integration, and a strong trajectory for future software‑driven improvements.

CTA: How to Move Forward with the Intuitive 490206 Vision Probe

If your institution is considering a robotic bronchoscopy upgrade or evaluating whether to standardize on the Intuitive 490206 Enhanced Vision Probe Instrument, start by aligning clinical goals with technology capabilities. Engage interventional pulmonologists, thoracic surgeons, and bronchoscopy suite managers to define target use cases, from high‑risk screening patients to complex nodules requiring precise navigation.

Next, collaborate with biomedical engineering, procurement, and financial stakeholders to map out lifecycle costs, anticipated case volumes, and potential reductions in downstream procedures. Validate that your Ion systems meet or exceed the required software versions and that your imaging environment can support integrated or adjunctive modalities that complement the enhanced vision probe.

Finally, design an implementation plan that includes hands‑on training, proctoring for early cases, and ongoing performance review. With structured planning and strong stakeholder alignment, the Intuitive 490206 Enhanced Vision Probe Instrument can be leveraged to its full potential, delivering better visualization, higher diagnostic confidence, and a more advanced standard of care for patients undergoing minimally invasive procedures for peripheral lung disease.

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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.