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Is the GE Vscan Air SL HANDHELD ULTRASOUND the right choice for modern point‑of‑care imaging?

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The GE Vscan Air SL handheld ultrasound brings a new level of wireless, dual‑probe imaging to the bedside, enabling rapid cardiac and vascular assessments with high‑resolution images in a truly portable form. For clinics and practices looking to adopt or upgrade to a compact, flexible POCUS platform, this device represents a significant step forward in workflow efficiency and diagnostic confidence at the point of care.

How is the current point‑of‑care ultrasound market evolving?

Handheld ultrasound has moved from a niche tool to a standard in emergency medicine, cardiology, critical care, and ambulatory settings. Data from MarketsandMarkets shows that the global POCUS market is projected to grow from about $4.2 billion in 2023 to over $7.5 billion by 2028, driven by demand for faster, bedside decision‑making and declining device costs. Adoption is no longer limited to hospitals; primary care, urgent care, and even solo practitioners are integrating POCUS into routine exams.

Deployment rates remain below potential, however, because many practices still rely on bulky, shared cart‑based systems or outdated handhelds with limited capabilities. This gap between clinical need and available tools creates a missed opportunity to improve triage, reduce unnecessary imaging, and deliver care in more resource‑constrained environments. As a result, many providers are searching for a modern, reliable, and truly portable solution that can handle both cardiac and vascular studies without switching devices.

What are the main pain points in current POCUS workflows?

Clinics and mobile providers often struggle with three core issues: limited portability, workflow interruption, and inconsistent image quality. Traditional cart‑based systems are too heavy and cumbersome to bring into every room, so ultrasound is often reserved only for specific “high‑acuity” cases instead of being used routinely. Even when a device is available, staff must spend time connecting probes, adjusting presets, and troubleshooting cables and charging, which slows down patient flow.

Another major pain point is having to use multiple devices or probes for different exams. A practice that needs both cardiac and vascular imaging typically owns at least two separate probes (sector and linear) and must disconnect/reconnect them between patients or even during the same exam. This not only reduces efficiency but also increases the risk of probe damage and cross‑contamination. In urgent settings, such delays can directly impact patient outcomes.

Finally, image quality and training barriers remain significant. Many clinics purchase entry‑level handhelds that lack the penetration, resolution, and advanced Doppler capabilities needed for reliable cardiac assessment. This forces clinicians to rely on more expensive imaging (echocardiography, CT, MRI), which increases costs and waiting times. At the same time, the lack of standardized training and poor support makes it difficult for non‑specialists to use POCUS effectively and confidently.

Why are traditional solutions still falling short?

Most legacy POCUS systems are built around a cart‑based, multi‑probe architecture that is not optimized for true point‑of‑care use. These systems require a dedicated operator, consume valuable floor space, and suffer from long startup and warm‑up times. They are also expensive to acquire and maintain, especially when multiple probes and service contracts are factored in, making them a poor fit for smaller practices or those with limited capital budgets.

Even newer handheld devices often fail to solve the core workflow problem: they are single‑probe or require frequent manual swapping. This forces clinicians to carry multiple devices or constantly change probes, which breaks the natural flow of a patient encounter. In fast‑paced environments like emergency departments or ambulatory care, this extra step can be the difference between timely intervention and a delayed diagnosis.

Battery life and ruggedness are additional shortcomings. Many handhelds offer only 30–40 minutes of continuous scanning, which is insufficient for a full shift, and they are not designed for harsh environments (e.g., ambulances, field settings). Poor waterproofing and impact resistance also increase the risk of damage and downtime, further raising the total cost of ownership.

How does the GE Vscan Air SL solve these challenges?

The GE Vscan Air SL is a wirelessly connected, dual‑probe handheld ultrasound that integrates a sector phased array and a linear array transducer into a single, compact device. This means clinicians can switch seamlessly between cardiac and vascular imaging without plugging in or changing probes, preserving workflow continuity at the bedside. The system is designed from the ground up for point‑of‑care use, with a focus on portability, image quality, and ease of use.

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Key capabilities include B‑mode, Color Doppler, M‑mode, and Pulsed Wave Doppler, enabling structured cardiac exams (e.g., LV function, pericardial effusion) and detailed vascular assessments (e.g., DVT, venous access, carotid). The device supports up to about 50 minutes of continuous scanning on a full charge, with wireless charging for convenience, and it can be paired with a mobile device via the Vscan Air app for real‑time viewing, image capture, and sharing.

GE’s XDclear transducer technology delivers high penetration and resolution across a broad range of patient sizes and anatomies, making it suitable for adult, pediatric, and neonatal cardiac and vascular studies. The system is also built to withstand demanding environments, with a rugged, waterproof housing that meets military‑grade drop and environmental standards, so it can be used reliably in ambulances, air‑rescue units, and field clinics.

What are the practical advantages of the Vscan Air SL vs. traditional handhelds?

Feature Traditional POCUS / Handheld Systems GE Vscan Air SL
Probe configuration Single probe or manual probe swapping Dual‑probe (sector + linear) in one device
Portability Often bulky cart or single handheld True handheld, wireless, pocket‑sized
Workflow Requires disconnecting/connecting probes No manual probe change between cardiac and vascular exams
Imaging modes Often limited to B‑mode and basic Doppler B‑mode, Color Doppler, M‑mode, PW Doppler
Image quality Variable, may lack penetration on larger patients High penetration/resolution with XDclear transducer tech
Battery life Typically 30–40 min continuous scanning Up to about 50 minutes of scanning
Ruggedness Varies; often not waterproof or drop‑tested Waterproof, military‑standard drop‑tested
Connectivity USB or short‑range wireless Bluetooth wireless to mobile device, cloud‑enabled features
Total cost of ownership High with multiple probes and service contracts Lower TCO with integrated dual‑probe design and fewer accessories

For clinics that currently rely on older handhelds or multiple probes on a cart, upgrading to the Vscan Air SL can significantly reduce time per exam, improve consistency of imaging, and make bedside POCUS truly practical for routine use.

How does GE equip the Vscan Air SL for real‑world clinical workflows?

GE has built several workflow‑oriented features into the Vscan Air SL platform to streamline daily use. The device connects wirelessly to a smartphone or tablet via the Vscan Air app, allowing images to be viewed in real time, captured, and shared securely. Presets for common exams (cardiac, vascular, lung, abdominal, etc.) help standardize scanning and reduce the need for manual optimization, which is especially helpful for generalists or less experienced users.

The user interface is designed for single‑thumb operation, with key controls like freeze, store, gain, and depth accessible through simple gestures. This minimizes the need to look away from the patient or struggle with complex menus during an exam. The system also supports auto‑EF (automatic left ventricular ejection fraction calculation) and other AI‑assisted tools (sold separately) to assist with structured cardiac exams and improve reproducibility.

On the backend, GE provides cloud‑based support resources, including clinical education materials, remote assistance, and software updates, which help maintain performance and keep clinicians up to date with best practices. For organizations managing multiple devices, the Vscan platform offers centralized management options that simplify device tracking, software version control, and compliance with security policies.

How can ALLWILL help practices adopt and maintain the Vscan Air SL?

ALLWILL supports clinics looking to implement the GE Vscan Air SL as part of a broader POCUS strategy, not just as a standalone purchase. Through its Smart Center, ALLWILL provides inspection, repair, and refurbishment services for medical imaging equipment, ensuring that every Vscan Air SL (new or pre‑owned) meets strict performance standards before deployment. This reduces the risk of receiving a non‑functional or underperforming unit.

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ALLWILL’s vendor management system, MET, connects practices with vetted technicians and trainers who can support Vscan Air SL setup, configuration, and hands‑on training. Instead of relying on a single OEM channel, clinics gain access to a network of qualified experts who can help optimize workflows, troubleshoot connectivity issues, and ensure staff confidence in using the device effectively.

For clinics concerned about budget and long‑term costs, ALLWILL offers brand‑agnostic consultations and provides both new and professionally refurbished Vscan Air SL systems. Trade‑up programs allow practices to upgrade to the latest technology without expensive service contracts or recertification fees, making it easier to adopt modern POCUS today while planning for future advancements. With ALLWILL, the Vscan Air SL becomes not just a device, but part of a sustainable, supported POCUS ecosystem.

Can a provider use the Vscan Air SL in routine clinical practice?

Yes, the Vscan Air SL is designed for real‑world, day‑to‑day use across a wide range of clinical environments. The workflow is intentionally simple: power on the device, pair it with a compatible mobile device via Bluetooth, select the appropriate exam preset, and scan. Images and clips are captured with a single tap and can be stored locally or exported to EMR/clinical systems through secure channels.

For practices that want to standardize POCUS across multiple providers, the Vscan Air SL can be deployed with consistent protocols and presets, and the wireless app connection makes it easy to review and approve studies remotely. When combined with structured training and ongoing support (such as that coordinated through ALLWILL’s MET platform), the device becomes a reliable tool for rapid triage, procedural guidance, and follow‑up assessments in cardiac, vascular, lung, and abdominal imaging.

What does a typical Vscan Air SL implementation look like?

Implementing the Vscan Air SL typically follows a structured, step‑by‑step process to ensure clinical utility and staff adoption:

  1. Assessment & planning
    Define the primary use cases (e.g., cardiac triage, DVT, pleural effusion, vascular access) and identify the key users (physicians, APPs, nurses). ALLWILL can help with a needs assessment and recommend whether to start with a new or refurbished Vscan Air SL based on budget and workflow goals.

  2. Device acquisition & configuration
    Acquire the Vscan Air SL (new or refurbished from a trusted source like ALLWILL) and configure the mobile device (iOS/Android) with the Vscan Air app. Set up user accounts, security policies, and network access as needed.

  3. Training & protocol development
    Conduct hands‑on training for users, focusing on probe handling, exam presets, basic image optimization, and interpretation basics. Develop simple protocols (e.g., “Cardiac FAST” or “DVT screen”) to standardize scanning and reporting.

  4. Integration into workflow
    Embed POCUS into routine workflows—for example, as part of the admission exam in the ER, pre‑op assessment, or post‑procedure follow‑up. Track usage and outcomes to quantify impact on decision‑making and efficiency.

  5. Support & maintenance
    Establish a maintenance plan with regular performance checks, software updates, and access to technical and clinical support through ALLWILL’s Smart Center and MET network. This ensures long‑term reliability and continuous improvement.

By following this process, clinics can move from “having a handheld ultrasound” to routinely using the Vscan Air SL as an integral part of patient care.

How can the Vscan Air SL be used in different clinical settings?

1. Community clinic / primary care

  • Problem: A primary care provider suspects heart failure in a patient with dyspnea but needs rapid assessment before referral.

  • Traditional approach: Schedule a formal echo, wait days to weeks, and manage symptoms empirically in the interim.

  • With Vscan Air SL: Perform a quick bedside cardiac exam to assess LV function, presence of pericardial effusion, and pleural effusion.

  • Key benefit: Faster risk stratification, earlier referral to cardiology, and more confident initial management without unnecessary imaging.

2. Emergency department / urgent care

  • Problem: An acutely ill patient presents with chest pain, hypotension, and possible tamponade or massive PE.

  • Traditional approach: Rely on clinical gestalt until a formal echo or CT is performed, which can take hours.

  • With Vscan Air SL: Perform a focused cardiac and lung exam at triage to detect pericardial effusion, RV strain, and pleural effusion, guiding immediate interventions.

  • Key benefit: Earlier detection of life‑threatening conditions, reduced time to critical decisions, and better resource utilization.

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3. Critical care / ICU

  • Problem: A critically ill patient requires repeated vascular access attempts, increasing the risk of complications.

  • Traditional approach: Blind or landmark‑based access, often requiring multiple attempts and potentially leading to pneumothorax or hematoma.

  • With Vscan Air SL: Use real‑time linear array imaging for US‑guided cannulation of central veins, reducing attempts and complications.

  • Key benefit: Higher first‑pass success rate, lower complication rates, and improved patient safety.

4. Mobile / field medicine

  • Problem: A rural or disaster‑response team needs to triage patients but lacks access to cart‑based ultrasound.

  • Traditional approach: Use only clinical assessment, which can miss significant pathology.

  • With Vscan Air SL: Perform rapid cardiac and vascular exams in the field to identify shock states, DVT, and free fluid, directing transport and treatment priorities.

  • Key benefit: Enhanced diagnostic capability in resource‑limited environments, supporting better triage and outcomes.

Why is now the right time to adopt the Vscan Air SL?

Portable ultrasound is no longer an “optional” add‑on; it has become a standard of care in many specialties, and delayed adoption increasingly puts practices at a competitive and clinical disadvantage. With rising patient expectations for rapid diagnostics and value‑based care, the ability to perform immediate, bedside imaging directly impacts throughput, patient satisfaction, and reimbursement.

The Vscan Air SL specifically addresses the key barriers to adoption: limited portability, workflow disruption, and inconsistent image quality. By consolidating cardiac and vascular imaging in a single, rugged, wireless device, it makes POCUS practical and sustainable for daily use, not just for academic centers but also for community clinics, urgent care, and mobile providers.

For practices that want to invest wisely, ALLWILL offers a clear path to implement the Vscan Air SL without overextending capital. Whether sourcing a new system or a professionally refurbished unit, ALLWILL provides the inspection, training, and long‑term support needed to ensure that the Vscan Air SL delivers reliable, high‑quality imaging for years to come.

How can I evaluate the Vscan Air SL before buying?

Is the Vscan Air SL suitable for both cardiac and vascular exams?
Yes, the Vscan Air SL has both a sector phased array probe (for cardiac and deep structures) and a linear array probe (for vascular, soft tissue, and superficial structures) in one handheld device, allowing seamless switching between cardiac and vascular imaging without changing probes.

Can I use it for procedures like vascular access or nerve blocks?
Yes, the linear array probe provides high‑resolution imaging suitable for real‑time guidance of vascular access, fluid drainage, nerve blocks, and other superficial procedures, making it a true multi‑application tool.

How long does the battery last in real use?
The device supports up to about 50 minutes of continuous scanning on a full charge, with wireless charging available. In typical clinical use, this is sufficient for a full shift or multiple patient exams.

Is it rugged enough for field or ambulance use?
Yes, the housing is waterproof and designed to meet military‑grade drop and environmental standards, so it can be used reliably in ambulances, air‑rescue, and field settings.

How do I manage training and support for my team?
GE provides clinical education materials and app‑based support, and partners like ALLWILL can connect clinics with vetted technicians and trainers through their MET platform to ensure hands‑on training and ongoing technical assistance.

Where can I find more detailed information?

Sources:

  • GE HealthCare – Vscan Air SL product page

  • GE HealthCare – Vscan Air SL technical specifications / datasheet

  • MarketsandMarkets – Point‑of‑Care Ultrasound Market Report

  • GEHealthcare.com – Vscan handheld ultrasound systems overview

  • GE Vscan support center and educational resources

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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.