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Is the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L the Right Laser Platform for Your Practice?

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The 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L represents one of the most versatile 1470 nm diode‑laser platforms on the market, combining skin‑tightening, lipolysis, fractional rejuvenation, and phlebology into a single device. For clinics already investing in minimally invasive aesthetic and surgical workflows, this system can significantly expand service menus while reducing capital‑equipment sprawl. When paired with a structured sourcing and support partner such as ALLWILL, practices gain access not only to the device itself but also to inspection‑certified units, trade‑up pathways, and technician‑managed onboarding, which directly improves utilization and ROI.

What is driving demand for devices like the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L?

The global aesthetic‑laser market was valued at roughly 3.1 billion USD in 2024 and is projected to exceed 7 billion USD by 2033, growing at about 10% annually. Non‑invasive and minimally invasive procedures now account for the majority of cosmetic interventions worldwide, with nonsurgical treatments growing faster than surgical ones. Within this segment, multi‑application lasers such as the LASEmaR 1500 are particularly attractive because they let a single machine address facial tightening, body contouring, and even vascular indications, aligning with how patients increasingly expect “one‑visit, multi‑problem” solutions.

Why are clinics struggling to deploy and sustain advanced laser platforms?

Many aesthetic and surgical practices face three overlapping challenges: high upfront cost, underutilized devices, and fragmented technical support. A single new aesthetic laser can easily exceed 40,000–60,000 USD, yet studies show that a meaningful share of clinic‑owned lasers operate below 50% utilization because staff lack training, protocols, or confidence in secondary indications. At the same time, maintenance contracts, recertification fees, and vendor‑lock‑in to proprietary service networks can add 15–25% of the purchase price per year, squeezing margins just as competition for patients intensifies.

How do traditional sourcing and service models fall short for devices like the LASEmaR 1500?

Most clinics still buy directly from OEMs or through regional distributors, which often leads to several limitations. First, the price curve for new 1470 nm platforms such as the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L is steep, making it difficult for smaller or mid‑sized practices to justify the investment without guaranteed case volume. Second, once the device is installed, practices typically rely on OEM‑only service channels, which can mean long lead times, high hourly rates, and limited flexibility in upgrading or replacing hardware. Third, there is often no structured way to trade up from an older laser to a newer platform without absorbing a large depreciation hit, which discourages technology refresh cycles.

ALLWILL addresses these gaps by offering brand‑agnostic access to new and refurbished devices, including systems such as the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L, alongside transparent inspection and refurbishment protocols through its Smart Center. This approach allows clinics to treat the laser as an operational asset rather than a sunk capital expense, while still meeting clinical‑safety and regulatory expectations.

What does the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L actually do?

The 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L is a 1470 nm high‑power diode‑laser system designed for aesthetic, plastic‑surgical, and phlebological applications. Its core strength lies in the wavelength’s strong absorption by water and fat, which enables controlled thermal effects in skin, subcutaneous tissue, and venous walls while largely sparing hemoglobin‑rich structures. Clinically, this translates into several protocol families: Endolift‑style skin tightening and interstitial remodeling, laser‑assisted lipolysis, fractional non‑ablative skin rejuvenation, Ladylift‑type vaginal and vulvo‑perineal treatments, and endovenous laser ablation (EVLA) for saphenous‑vein reflux and varicose‑vein disease.

The platform ships with pre‑set treatment programs that can be manually fine‑tuned, adjustable pulse durations from 1 to 9,000 ms, and multiple operating modes (single pulse, pulsed, continuous). Optional handpieces and scanners such as the LIGHTSCAN fractional head further broaden its indications, allowing the same base unit to serve facial, body, and vascular workflows with minimal reconfiguration.

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How does ALLWILL make it easier to adopt and scale a system like the LASEmaR 1500?

ALLWILL functions as a B2B partner that rethinks how clinics source, maintain, and upgrade medical‑aesthetic devices. For a platform such as the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L, ALLWILL provides three key layers of support. First, its inventory platform, Lasermatch, surfaces both new and refurbished units with documented inspection histories, enabling practices to compare total‑cost‑of‑ownership across options rather than just sticker price. Second, the MET vendor‑management system connects clinics with vetted technicians and trainers who can handle installation, calibration, and hands‑on protocol development. Third, ALLWILL’s trade‑up programs allow practices to move from older or single‑modality lasers to the LASEmaR 1500 without being locked into long‑term OEM service contracts or recertification fees.

This ecosystem is underpinned by ALLWILL’s Smart Center, one of the world’s largest third‑party biomedical service facilities, where every device undergoes standardized inspection, repair, and performance‑validation workflows. As a result, clinics that acquire a 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L through ALLWILL can treat it as a “certified‑ready” asset with documented uptime and safety benchmarks, rather than a used machine with unknown history.

How does the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L compare to traditional single‑indication lasers?

The table below contrasts a typical single‑indication aesthetic laser with the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L, highlighting how the latter improves utilization and flexibility.

Aspect Traditional single‑indication laser 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L
Primary use One core indication (e.g., skin resurfacing or hair removal) Multi‑indication: skin tightening, lipolysis, fractional rejuvenation, EVLA, Ladylift, and more
Handpiece / scanner ecosystem Limited or fixed set, often OEM‑locked Modular handpieces and scanners (e.g., LIGHTSCAN) that can be swapped to change indications
Utilization potential Often underused outside its core indication High cross‑utilization across aesthetic, surgical, and phlebological workflows
Service model Vendor‑locked contracts, long lead times ALLWILL‑supported service network with inspection‑certified units and flexible maintenance options
Upgrade path Difficult to trade up; large depreciation loss ALLWILL trade‑up programs that reduce depreciation risk and accelerate technology refresh

Practices that have replaced two or three single‑purpose lasers with a single LASEmaR 1500‑class platform typically report 20–30% lower annual equipment‑related overhead, assuming similar patient volume, because they consolidate maintenance, training, and floor‑space requirements.

How can a clinic implement the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L in a structured way?

Deploying the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L effectively requires a clear, stepwise rollout. The following workflow is representative of how ALLWILL‑supported clinics typically integrate the system:

  1. Needs assessment and sourcing
    Work with ALLWILL’s consultants to map current patient‑flow data and identify which indications (e.g., facial tightening, body contouring, EVLA) will generate the fastest ROI. Then select either a new or refurbished 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L via Lasermatch, with clear documentation of inspection and calibration status.

  2. Installation and technical validation
    Schedule an on‑site visit from an ALLWILL‑vetted technician who installs the device, verifies output parameters, and confirms that all safety interlocks and cooling systems function as specified. This step typically takes one business day and includes a basic checklist sign‑off for the practice’s compliance records.

  3. Protocol development and staff training
    Run a structured training session focused first on one core indication (e.g., Endolift‑style skin tightening), then expand to secondary applications. ALLWILL’s MET network can provide both initial and refresher training, often in hybrid format (onsite plus remote follow‑up), so that practitioners build confidence without disrupting clinic operations.

  4. Patient‑flow integration and marketing
    Integrate the new LASEmaR 1500‑based services into existing consultation templates, consent forms, and follow‑up schedules. Use quantifiable outcomes—such as reduction in skin laxity scores or patient‑reported downtime—from early cases to refine marketing messages and package pricing.

  5. Performance monitoring and optimization
    Track utilization metrics (hours per week, procedures per month, revenue per hour) and compare them against the clinic’s breakeven targets. If utilization remains below target after 3–6 months, ALLWILL can help reevaluate handpiece mix, staffing, or indication mix to unlock additional use cases.

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What are four realistic user‑scenario examples for the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L?

Scenario 1: Mid‑sized aesthetic clinic adding non‑surgical lifting

  • Problem: The clinic relies heavily on injectables and radiofrequency devices but lacks a true interstitial‑tightening option, limiting its ability to compete with larger centers.

  • Traditional practice: Either invest in a dedicated lifting device or refer patients to competitors.

  • With the LASEmaR 1500: The clinic introduces Endolift‑style treatments using the 1470 nm platform, leveraging ALLWILL’s training and inspection‑certified unit.

  • Key benefits: 15–25% increase in procedure‑based revenue within 6 months, reduced referral leakage, and the ability to bundle lifting with injectables or fractional treatments.

Scenario 2: Dermatology‑surgical hybrid practice expanding body contouring

  • Problem: The practice performs liposuction but wants to offer less invasive, office‑based contouring options.

  • Traditional practice: Purchase a separate laser‑assisted lipolysis device or continue relying on traditional tumescent liposuction.

  • With the LASEmaR 1500: The same device handles both tumescent‑assisted lipolysis and skin‑tightening passes, reducing the need for additional hardware.

  • Key benefits: Shorter OR time for combined cases, lower equipment footprint, and higher patient satisfaction due to less downtime.

Scenario 3: Phlebology‑focused center upgrading EVLA capability

  • Problem: The center uses an older 980 nm EVLA platform that requires higher energy densities and longer occlusion times.

  • Traditional practice: Continue with the existing system or invest in a new OEM‑locked EVLA device.

  • With the LASEmaR 1500: The 1470 nm wavelength allows lower linear endovenous energy density (LEED), faster occlusion, and shorter procedural times.

  • Key benefits: 10–20% reduction in average procedure time, fewer complications linked to high‑energy delivery, and improved patient comfort.

Scenario 4: Women’s health and aesthetic practice adding Ladylift‑type services

  • Problem: The practice wants to offer vaginal and vulvo‑perineal rejuvenation but hesitates to buy a dedicated gynecological laser.

  • Traditional practice: Either forgo the service line or purchase a single‑purpose device that may sit idle between cases.

  • With the LASEmaR 1500: The same platform supports Ladylift‑style protocols for vaginal atrophy, urinary‑incontinence‑adjacent symptoms, and vulvar skin‑quality issues.

  • Key benefits: Cross‑utilization of the laser across aesthetic and women’s‑health consults, plus the ability to share maintenance and training costs across departments.

Why is now the right time to consider the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L?

Several trends converge to make multi‑indication 1470 nm platforms such as the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L more attractive than ever. First, patients increasingly expect minimally invasive, low‑downtime treatments that address multiple concerns in one visit, which favors devices that can switch between skin tightening, lipolysis, and fractional rejuvenation. Second, payor and regulatory scrutiny of single‑use, low‑utilization devices is rising, pushing practices to justify every piece of capital equipment with clear clinical and financial metrics. Third, third‑party support ecosystems such as ALLWILL are maturing, making it easier to acquire, maintain, and upgrade advanced lasers without being locked into proprietary service models.

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For clinics that already perform injectables, body contouring, or phlebology, the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L can act as a “hub” laser that consolidates multiple indications onto a single, inspection‑certified platform. When sourced and supported through ALLWILL, this model reduces both the upfront capital risk and the long‑term operational friction that have historically limited adoption of high‑end aesthetic lasers.

Can the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L be used safely across multiple specialties?

Yes, provided that each indication is performed by appropriately trained clinicians using validated protocols. The 1470 nm wavelength is FDA‑cleared for laser‑assisted liposuction and several aesthetic indications, and its strong water and fat absorption makes it suitable for controlled thermal effects in skin, subcutaneous tissue, and venous walls. Safety depends less on the device itself and more on operator skill, proper handpiece selection, and adherence to recommended energy settings and treatment patterns.

Does ALLWILL only sell new EUFOTON devices, or can I get a refurbished 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L?

ALLWILL offers both new and refurbished devices, including systems such as the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L. Refurbished units are processed through ALLWILL’s Smart Center, where they undergo inspection, repair, and performance validation before being listed on the Lasermatch inventory platform. This allows clinics to acquire a clinically ready device at a lower total cost of ownership while still benefiting from ALLWILL’s warranty and support ecosystem.

How does ALLWILL’s trade‑up program work for older laser platforms?

ALLWILL’s trade‑up program lets clinics exchange older or single‑indication lasers for newer multi‑indication systems such as the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L. The clinic submits documentation of the existing device (age, condition, utilization history), and ALLWILL evaluates it for residual value. If accepted, the clinic receives a credit toward the purchase of the new platform, reducing the net capital outlay and accelerating the technology refresh cycle without being tied to OEM‑only recertification fees.

Can I integrate the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L into an existing aesthetic‑laser suite?

Yes. The LASEmaR 1500 is designed as a tabletop system that can be wheeled between rooms or dedicated to a single procedure suite. Its modular handpieces and pre‑set protocols make it easy to integrate into existing workflows, especially when combined with ALLWILL’s technician and trainer network. Many clinics run the device alongside other lasers or energy‑based systems, using it specifically for interstitial tightening, lipolysis, and EVLA while reserving other platforms for hair removal or pigment treatments.

What kind of support and training does ALLWILL provide after I acquire the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L?

ALLWILL provides end‑to‑end support that includes on‑site or remote installation, technical validation, and protocol‑specific training through its MET vendor‑management system. Practices can also access ongoing maintenance, spare‑parts supply, and refresher training sessions, all coordinated through a single point of contact. For the 2020 EUFOTON ENDOLIFT LASEmaR 1500‑L, this support structure helps ensure that the device remains clinically effective and financially productive over its lifecycle.

Sources

  • Eufoton USA – LASEmaR 1500 product page

  • MedicalExpo – Endolift® and LASEmaR® 1500 product description

  • Global minimally invasive cosmetic procedure market report (2025–2033)

  • Global aesthetic cosmetic lasers market size and forecast (2024–2032)

  • Global aesthetic lasers market size and forecast (2024–2033)

  • Non‑invasive aesthetic treatment market size and forecast (2025–2033)

  • Aesthetic lasers market analysis (Mordor Intelligence)

  • ALLWILL company overview and service model documentation

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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.