Knowledge

Sourcing EndyMed Pure for Aesthetic Practices: Clinical Mechanics, Technical Audits, and Commercial ROI

Posted on by Dr. Jacklove

The global demand for non-surgical aesthetic medical platforms continues to accelerate as modern clinics prioritize energetic devices that multi-task without inflating capital expenditures. The EndyMed Pure stands out in this competitive landscape by integrating professional skin tightening, body contouring, radiofrequency (RF) microneedling, and fractional skin resurfacing into a single, compact workstation. For aesthetic medical groups, dermatology practices, and medical spas looking to optimize device-driven revenue, this comprehensive guide analyzes the clinical positioning, asset evaluation metrics, secondary-market technical audits, and strategic procurement frameworks necessary for a secure, high-ROI acquisition.

Market Context and Professional Aesthetic Positioning

Recent industry reporting from 2024 through 2026 indicates a sustained macroeconomic shift toward minimally invasive skin-rejuvenation systems. The global aesthetic device market surpassed approximately USD 18.5 billion in 2025 and is projected to maintain strong growth momentum through 2030, driven heavily by non-surgical skin tightening demand. Medical practices face increasing pressure to provide highly localized, low-downtime treatments for the face, neck, and multi-zone body tightening. As clinic operational costs rise, multi-application platforms help practitioners manage space efficiency while catering to a broader patient demographic.

For commercial buyers researching an EndyMed Pure for sale, the decision logic extends beyond simple unit availability. The core evaluation centers on whether a single, compact radiofrequency platform can support multi-tier treatment menus without compromising energy delivery consistency, clinical safety, or operational workflow. Clinical studies indicate that premium RF-based treatments can improve dermal collagen density by up to 35% after structured treatment cycles, provided the hardware delivers consistent energy stability.

Technical Fundamentals and Core Handpiece Capabilities

The platform is engineered around proprietary 3DEEP RF technology, a multi-source, phase-controlled radiofrequency architecture. Unlike traditional mono-polar or bi-polar RF systems that can cause surface overheating or irregular energy scattering, this technology controls the interaction between multiple energy sources. It drives the electromagnetic energy deep into the dermal layers (targeting depths between 2.5 mm and 4.5 mm) while keeping the epidermal temperature profile predictable and safe, minimizing patient discomfort.

This precise deep-tissue thermal delivery triggers immediate collagen contraction and stimulates long-term neocollagenesis. The therapeutic outcome manifests as measurable tissue tightening, reduction of facial wrinkles, and improvement of structural laxity. Clinical RF treatments delivering stable dermal temperatures between 40 degrees Celsius and 45 degrees Celsius show up to 32% higher collagen remodeling efficiency compared to fluctuating thermal profiles.

The structural versatility of the platform is defined by its extensive handpiece and module ecosystem:

  • iFine Handpiece: Specially designed for delicate, hard-to-treat periorbital and perioral zones, targeting fine lines and laxity around the eyes and mouth with an expected power envelope of 10–20W.

  • Small / mini Shaper Modules: Optimized for localized facial contouring, submental tightening, and jawline definition, operating within a standard 20–40W range.

  • Shaper Handpiece: Engineered for larger body zones, delivering deep thermal energy via a 40–65W envelope combined with vacuum assist exceeding 250 mbar to support non-invasive body contouring, cellulite management, and skin firmness.

  • FSR (Fractional Skin Resurfacing) Module: Utilizes multi-source fractional ablation operating at 10–30W with pulsed RF energy (10–60ms delivery) to target post-acne scarring, epidermal texture roughness, and hyperpigmentation.

  • Intensif RF Microneedling Handpiece: Combines a non-insulated needle array with smooth, motorized insertion technology to deliver targeted RF heat deep within the dermis, serving as a gold standard for traumatic scars, deep wrinkles, and stretch marks.

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Commercial Logic: Maximizing Asset Utilization and ROI

In a professional medical setting, medical equipment should be evaluated as an active revenue platform rather than just a capital asset. Clinical buyers regularly encounter distinct operational bottlenecks when scaling their services, which multi-application technology is uniquely positioned to solve.

The greatest risk in aesthetic technology procurement is capital fragmentation. A clinic that purchases separate standalone systems for wrinkle reduction, skin resurfacing, and body contouring faces multiplied up-front acquisition costs, redundant staff training certifications, and excessive physical footprint requirements. Inconsistent thermal penetration from lower-tier generic systems can force practitioners to extend treatment times by up to 20%, reducing daily patient capacity and diminishing financial returns.

Furthermore, standalone point-solution devices regularly suffer from seasonal underutilization. By utilizing a platform that spans across face, neck, body, scar, and stretch-mark protocols, an administrative team can cross-sell services and smooth out treatment demand across the calendar year. For instance, a patient undergoing a facial tightening protocol can easily be converted into a body contouring package during the same room-booking window, maximizing chair utilization rates and accelerating the timeline to achieve a complete return on investment.

Comparative Framework: Platform vs. Point Solutions

To assist clinical procurement managers in assessing the competitive landscape, the following matrix compares the multi-application platform approach against standard single-purpose alternatives.

Evaluation Metric EndyMed Pure Platform Alternative 1: Single-Purpose Tightening Unit Alternative 2: Basic Standalone Microneedling
Core Operational Profile Multi-application RF workstation Dedicated single-indication system Needle-focused mechanical treatment
Treatment Breadth Tightening, body contouring, RF microneedling, fractional resurfacing Isolated skin tightening or localized heating Texture, acne-scarring, and superficial remodeling
Energy Stability Profile Multi-source controlled RF with impedance monitoring Single-source RF fluctuation risks Variable or non-RF mechanical penetration
Dermal Penetration Continuity Up to 4.5 mm consistent depth control Variable 2–3 mm heating depths Restricted to mechanical needle depth
Spatial and Room Efficiency High; compact footprint replaces up to three separate devices Variable; often requires dedicated treatment room setup Compact; limited structural integration with other modalities
Maintenance Cycle Metrics Extended operational stability intervals Frequent recalibration (every 300–500 hours) High mechanical wear on modular motors
Primary Institutional Fit Versatile workhorse for growing and multi-room clinics Specialized centers with highly concentrated patient volume Practices focused primarily on scar revision and texturing

Strategic Sourcing Scenarios for Medical Practices

To understand how this asset functions within an active practice, consider these three distinct implementation pathways deployed across different clinical models:

Facial Tightening Center Expansion

  • Traditional Workflow: The practice procures one dedicated mono-polar machine for deep tissue lifting and a separate laser system for epidermal texture refinement.

  • Platform Workflow: The clinic deploys a single workstation equipped with both the iFine and FSR handpieces. The practitioner addresses deep dermal laxity and superficial micro-ablation within a unified appointment, optimizing clinical labor hours and reducing device switching time.

Medical Spa Expanding Into Body Services

  • Traditional Workflow: The provider invests heavily in high-cost, high-footprint fat-reduction or body-sculpting hardware, requiring dedicated rooms and long patient setup protocols.

  • Platform Workflow: Management utilizes the Shaper and mini Shaper modules on their existing platform. This strategy expands the service menu into non-surgical body tightening and contouring without committing to secondary high-overhead lease agreements.

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Scar Revision and Texture Specialization

  • Traditional Workflow: The clinical team relies on manual microneedling pens or non-RF fractional lasers, resulting in extended downtime or limited treatment efficacy for deep fibrotic tissue.

  • Platform Workflow: The medical team adopts the Intensif RF microneedling handpiece. The integration of gold-plated needle deployment with deep, controlled RF thermal energy delivery creates a more effective therapeutic pathway for tough acne scars and stretch marks, increasing client retention and premium package sales by offering higher patient comfort profiles.

Technical Audit Framework and Secondary-Market Diligence

Whether your organization is evaluating a factory-new unit or navigating the secondary market for a pre-owned or refurbished system, executing a deep technical audit is vital. Searching for an EndyMed Pure for sale often looks straightforward until procurement teams realize the platform’s real value depends less on the console itself and more on whether its multi-handpiece ecosystem is intact, properly calibrated, and fully authorized by the core software.

The 3DEEP phase-controlled RF engine relies on a 6-channel generator designed to distribute energy across multiple electrode pairs. A console may pass a basic power-on test yet still exhibit uneven delivery if internal channel calibration has drifted or if specific internal components are degraded. This is particularly relevant in pre-owned setups where prior repairs may affect how applicators communicate with the generator under a live load.

A rigorous procurement due-diligence audit must incorporate the following verification steps:

  • RF Channel Stability and Calibration: Demand documented diagnostic testing verifying uniform energy dispersion across all 6 channels without internal power drops.

  • Intensif Mechanical Drive Validation: Test the Intensif handpiece under an extended cycling sequence. Verify that motorized needle penetration depth corresponds exactly to physical settings and that the motor maintains stable insertion speeds without intermittent electrical faults.

  • Software Recognition and License Authorization: Confirm that all included handpieces are fully recognized by the console software without throwing error codes, jumping into restricted operational modes, or triggering usage counters and lockout mechanisms.

  • FSR Pulse Timing Accuracy: Verify that fractional pulse durations remain stable within the 10–60 millisecond range to prevent superficial overheating or uneven tissue abrading.

  • Vacuum System Integrity: Inspect the Shaper handpiece lines to ensure vacuum stability exceeding 250 mbar for uniform suction during body protocols.

  • Physical Interface and Connectors: Examine all cables, strain reliefs, and connector pins for micro-fractures or intermittent connection drops caused by improper handling.

  • Regulatory and Serial Alignment: Verify the physical serial number and manufacture year against original manufacturer registries to confirm regulatory compliance and future firmware update support.

Strategic Value Realization with ALLWILL

The primary operational friction in aesthetic medical procurement is navigating the gap between equipment sourcing and long-term asset maintenance. Traditional medical device vendors often function purely as sales channels, leaving clinics to independently navigate technical calibration, parts replacement, handpiece sourcing, and workflow optimization.

ALLWILL Group resolves these systemic inefficiencies by operating as a dedicated B2B equipment solutions partner. Through its centralized support model encompassing the Smart Center infrastructure, the MET technician network, and the specialized Lasermatch inventory platform, ALLWILL handles the complex verification paths required for platforms like the EndyMed Pure. Rather than managing a blind transactional purchase, buyers are empowered to evaluate new and certified refurbished options side by side with full transparency.

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By coordinating independent technical inspections, facilitating applicator replacements, and offering clear trade-up pathways, ALLWILL helps practices minimize operational downtime. This systematic oversight ensures that the selected device configuration aligns directly with the clinic’s treatment volume and long-term service planning, turning hardware acquisition into a scalable corporate asset.

ALLWILL Clinical & Technical Insights

“In the business of B2B medical aesthetics, true asset value is not determined by an isolated headline feature or an aggressive promotional price on a secondary market marketplace. Long-term profitability depends on how seamlessly a platform integrates with a clinic’s existing staff workflow, local patient demographic demands, and core technical support infrastructure. The EndyMed Pure represents an exceptionally intelligent acquisition for modern multi-room facilities—provided that the buying committee evaluates technical calibration, RF channel stability, and handpiece software authorization with the exact same rigor applied to the upfront purchase price. Maximizing clinical ROI requires moving past basic vendor transactions and grounding procurement decisions in verifiable inspection data, continuous technical documentation, and structured post-sale operational support.”

Frequently Asked Questions

What are the primary technical advantages of buying an EndyMed Pure with 3DEEP technology?

The main advantage is access to a multi-application RF platform capable of supporting diverse treatment categories within a single console. The phase-controlled 3DEEP architecture allows clinics to consolidate equipment footprint and reduce capital costs, but real-world performance depends heavily on channel stability and applicator integrity.

Is this multi-application platform appropriate for space-constrained clinics?

Yes, the system is engineered with a compact physical footprint specifically to optimize high-traffic treatment rooms. It allows multi-room aesthetic practices to offer an extensive array of face and body procedures without taking up valuable floor space with multiple single-purpose machines.

How can a clinic verify calibration on a pre-owned Intensif handpiece?

Calibration must be assessed by observing motor consistency across repeated cycles and comparing selected needle depths with actual physical penetration. Any speed instability, mechanical lagging, or software pairing mismatch indicates internal wear and the immediate need for professional servicing.

What operational risks exist regarding applicator software recognition?

Many secondary-market listings underrepresent software-level restrictions. Certain handpieces may trigger error codes or enter restricted operational modes if the console firmware is incompatible or if specific usage lockout mechanisms are active. Buyers must confirm that all handpieces are fully unlocked and recognized by the generator prior to completing procurement.

How often does the EndyMed Pure system require standard maintenance?

Premium RF platforms are built for extended operational intervals, typically extending maintenance cycles beyond 500 operational hours. However, regular verification of impedance response curves and daily system checks are recommended to maintain uniform energy dispersion across target zones.

What ambient room conditions optimize EndyMed Pure treatment workflows?

Practices should maintain ambient treatment room temperatures between 20 degrees Celsius and 24 degrees Celsius. This controlled environment ensures consistent patient skin impedance readings and supports stable, predictable radiofrequency energy delivery throughout the session.

Dr. Jacklove

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        1.  EQUIPMENT AVAILABILITY. Equipment offered for sale by MRP is subject to availability. MRP shall not be liable to Buyer in case of stock outage or unavailability of the Equipment. MRP reserves the right to change the equipment offered for sale at any time and without notice to Buyer. Availability of equipment may be determined when an order is placed, and, if unavailable, MRP will inform Buyer of such unavailability, offer other available equipment as substitution or cancel the order. Such cancelled order will be refunded by MRP to Buyer, except for an order for a Special Order Product, which cannot be cancelled once the order is placed.

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        8.  MRP’S WARRANTIES, IF ANY.

(a) Equipment Sold “As Is.” UNLESS OTHERWISE STATED ON THE QUOTE OR IN A WRITING SIGNED BY AN MRP OFFICER, BUYER AGREES THAT THE EQUIPMENT SOLD IN THIS AGREEMENT IS BEING SOLD ON AN “AS IS,” “AS AVAILABLE” BASIS, SUBJECT TO SECTIONS 8(c) AND 9, AND HAVE NO WARRANTIES OR REPRESENTATIONS OF ANY KIND, WHETHER IMPLIED OR ARISING BY LAW, STATUTE OR OTHERWISE, INCLUDING, WITHOUT LIMITATION, ANY WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE OR USE, NON-INFRINGEMENT, WORKMANLIKE MANNER, QUALITY, ACCURACY, TITLE, AND/OR IMPLIED FROM A COURSE OF DEALING OR PERFORMANCE USAGE IN TRADE.

(b) Special Order Product. If this Agreement includes the sale of a product that MRP does not currently have or typically keep in stock, in MRP’s sole determination, but is acquired from a third party specifically for Buyer (a “Special Order Product”), then Buyer agrees that (i) Buyer, at its sole discretion, has made the selection of such Special Order Product, (ii) such Special Order Product is being acquired by MRP solely at the request of Buyer, (iii) no representation, warranty or guarantee has been made by MRP with respect to such Special Order Product, (iv) the obligation of Buyer to pay MRP for the Special Order Product is absolute and unconditional, and (v) Buyer waives and releases MRP from all claims, damages and losses arising out of such Special Order Product. Special Order Products carry no right to inspection before or after delivery, and MRP is not responsible for examining or evaluating such Special Order Products. MRP makes no warranty about Special Order Products and offerings of the third party (including description of the Special Order Product). MRP does not assume any responsibility or liability for the actions, product and content of all these and any other third parties. If there are any problems with any Special Order Product, Buyer must contact the manufacturer of such Special Order Product for assistance.

(c) Limited Warranties, If Any.

(i) If the Quote expressly states that the Equipment has a warranty for a certain time (a “Warranty Period”), then MRP warrants that the Equipment shall be in good working order under normal use for the Warranty Period, which Warranty Period shall commence from the date of delivery to Buyer (the “Delivery Date”), unless otherwise approved by an MRP Officer in writing, except for the following: (A) New (not used or pre-owned) Equipment that is to be serviced by MRP: if the Quote is silent, warranted to be in good working order under normal use for one hundred eighty (180) days from the Delivery Date; (B) Used Equipment sold refurbished by MRP: if the Quote is silent, warranted to be in good working order under normal use for thirty (30) days from the Delivery Date; (C) Consumable/disposable Equipment: if the Quote is silent, warranted to have been shipped from MRP in functional condition, and no additional warranty shall apply; no service shall be provided either. These items should be inspected for obvious damage, subject to Section 6 and 8(e), and MRP’s obligation under this warranty and this Section 8(c)(i)(C) is limited to replacement of the Equipment; and (D) New (not used or pre-owned) Equipment that is to be serviced by the manufacturer: if the Quote is silent, MRP makes no warranty for any such Equipment. Buyer’s sole warranty for any such Equipment, if any, shall be the original manufacturer’s warranty, which MRP agrees to pass on to Buyer, as applicable. (ii) For the limited warranties of Section 8(c)(i), including exceptions (A) and (B), but not (C) or this (D), Buyer is entitled to telephone, e-mail and video technical assistance and, subject to Sections 8(d) and 8(e), repair or replacement of such Equipment, in MRP’s sole discretion, should the Equipment become inoperative through normal use during the Warranty Period. Loaner equipment is not provided, but if so arranged by MRP, Buyer shall pay MRP the cash list price of any unreturned loaner equipment provided by MRP within seven (7) days of a written demand from MRP. (iii) Repair or replacement under any limited warranty of Equipment may be with parts or products that are new, used or refurbished, carrying the same limited warranty for the remaining term of the original item. Repairs or replacements shall not interrupt, extend or prolong the term of the warranty. (iv) For Services purchased under this Agreement, MRP warrants that the Services shall be performed using competent personnel in a professional manner in accordance with generally recognized industry standards for similar services. Subject to Sections 6 and 8(e) herein, if any Service was not performed in accordance with the aforementioned warranty, then MRP shall, in its sole discretion, either (A) repair or re-perform the applicable Service, or (B) credit or refund the price of such Service at the pro rata contract rate.

(d) Exclusions. MRP reserves the right, without liability, to void all warranties and remedies, including any obligation to service, repair, replace or otherwise remedy defects, errors or failures of the Equipment due to the occurrence of any of these events, and MRP shall be in no way responsible for: (i) handling, maintenance or use in a manner that is inconsistent with and/or contrary to the original manufacturer’s or MRP’s recommended procedures and/or instructions, including, without limitation, use of or with an unauthorized third-party good or part; (ii) any failure or damage resulting from negligence, alteration, modification or relocation of the Equipment by Buyer, its employees, agents or representatives; (iii) attempted or actual unauthorized dismantling, disassembling, service, repair, addition or change of the Equipment, including, without limitation, changing the serial number or shot count; (iv) abnormal wear and tear, including, without limitation, use under abnormal conditions (e.g., unclean, dusty, or exposure to extreme electromagnetic radiation, temperature or humidity); or (v) damage or failure of the Equipment due to a Force Majeure Event or a problem in the premises of the Equipment. In any of the above situations, or for any Equipment that has no warranty, MRP has sole discretion to service the Equipment, at Buyer’s expense, at MRP’s then-in-effect rates for service, labor, travel, shipping and materials.

(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.

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        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.