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Jeisys HIFU Cartridges: A Multi‑Depth Clinical Configuration & Cartridge Longevity Guide

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For clinic owners evaluating Jeisys‑type multi‑depth HIFU platforms, the core decision is how to configure D1.5–D13 mm cartridges by facial zone and indication while protecting consumable lifespan and treatment margins. Evidence‑based protocols typically use 1.5, 3.0, and 4.5 mm for layered facial tightening and 6–13 mm for body adipose targeting, with line counts per cartridge managed to balance clinical outcomes and cartridge cost per shot. The right mapping, maintenance, and usage policy will do more for long‑term ROI than chasing maximum energy per pass.

What Jeisys‑Type HIFU Does & Who It Is For

Multi‑depth HIFU platforms with cartridges from roughly 1.5 mm to 13 mm are designed for non‑invasive lifting, tightening, and localized adipose reduction by depositing focused ultrasound into targeted tissue planes. These systems typically offer facial applications (brow, midface, jawline) using 1.5–4.5 mm cartridges and body contouring using 6–13 mm cartridges.

They suit medical spas, aesthetic clinics, and dermatology practices that already have a foundational injectables or energy‑based portfolio and want to add a non‑surgical tightening option with modest consumable exposure compared with RF microneedling or cryolipolysis. High‑volume face and jawline work with a smaller but steady body‑contouring segment tend to see the best asset utilization. ALLWILL frequently sees HIFU adopted as a “bridge” between injectables and surgery for midlife patients seeking lift with minimal downtime.

Depth‑Driven Configuration: Mapping D1.5–D13 mm To Treatment Zones

Depth values and use‑cases here reflect common manufacturer and training‑manual practices for 7D/12D‑class systems equivalent to Jeisys multi‑depth platforms.

Facial Rejuvenation: 1.5, 3.0, and 4.5 mm

  • D1.5 mm: Superficial dermis, used around the periorbital area, superficial forehead, and fine lines where skin is thin.
  • D3.0 mm: Mid‑dermis, often used over cheeks, nasolabial region, and submalar zones for collagen stimulation and texture improvement.
  • D4.5 mm: SMAS‑level targeting over lower face and jawline for lifting and contouring, avoiding thin bony prominences such as zygoma and immediate periorbital rim.

A common training pattern is to begin with the deepest pass (4.5 mm), then 3.0 mm, then 1.5 mm, with slightly overlapping lines and attention to “forbidden zones” around major nerves. Protocols emphasize mapping and marking before treatment, using sliding or stamping modes based on patient discomfort and operator control.

Jawline Contouring: Depth Strategy

For non‑invasive jawline contouring, the goal is to combine SMAS tightening and modest subcutaneous heating without overdosing over bone:

  • Primary: 4.5 mm along the mandibular border and jowl area, keeping clear of the marginal mandibular nerve zone as per training diagrams.
  • Secondary: 3.0 mm over jowls and lateral lower face to support tightening of more superficial structures.
  • Optional: 1.5 mm in fine‑line or marionette‑line areas when skin thickness allows.

Practitioner manuals recommend stretching skin over bony areas (e.g., jawline) for patient comfort and to ensure consistent coupling, and avoiding direct treatment over the mandibular angle itself. This is particularly important when operators are tempted to “chase” sharper angles with extra passes.

Nasolabial Folds & Midface

For nasolabial folds and midface soft tissue, the emphasis is usually on 3.0 mm and 1.5 mm cartridges:

  • D3.0 mm: Workhorse depth for mid‑dermal tightening in the nasolabial and paranasal region.
  • D1.5 mm: Supplemental pass for superficial lines and perioral texture, avoiding vermilion border and areas with very thin skin.

Most device manuals advise avoiding direct shots over dental implants or using lower energy with appropriate gauze if treating near maxillary or mandibular dental work. This should be built into staff protocols and consent forms.

Body Contouring & Localized Adipose Reduction: 6–13 mm

For body contouring and localized adipose reduction with HIFU, multi‑depth cartridges around 6, 9, and 13 mm are used in descending depth order to thermally coagulate adipocytes in the subcutaneous fat layer while sparing overlying dermis.

  • D13 mm: Deeper subcutaneous adipose targeting in thicker areas such as abdomen or flanks.
  • D9 mm: Intermediate layer for more moderate adipose thickness.
  • D6 mm: Superficial subcutaneous fat or areas with less pinch thickness, still avoiding direct treatment over ribs, iliac crest, or other bony landmarks.
Also check:  Why Are Multimodal Protocols Driving Body Contouring in 2026?

Protocols stress avoiding bony areas and nerve‑rich regions, using reference images, and working from deep to superficial depths to minimize variability and overlap. Comparable adipose‑focused HIFU systems like Liposonix also target subcutaneous fat at around 8–13 mm, reinforcing this depth strategy.

Revenue, Utilization & Payback Math Around Cartridges

Because HIFU cartridge lines are finite (e.g., often around 10,000–20,000 lines per cartridge, depending on manufacturer), your primary economic lever is shots‑per‑protocol, not energy per shot. Each clinic’s actual numbers will vary, but you can structure your model around three variables:

  • Typical lines per full‑face protocol (often 350–550 lines, split across depths).
  • Cartridge line capacity (e.g., roughly 10,000 lines used in many 4‑in‑1 or 7D‑style systems).
  • Consumable cost per cartridge (new or refurbished) and per‑treatment margin.

For example, if you standardize a 400‑line facial treatment and a 10,000‑line cartridge, you are looking at approximately 25 full‑face patients per cartridge. If your blended consumable cost per cartridge is 600–900 USD (new or CPO), your per‑patient cartridge cost is roughly 24–36 USD, excluding device depreciation and staff time. These are estimates and must be calibrated to your vendor invoices and negotiated pricing.

From a payback standpoint, a clinic charging 600–900 USD per full‑face HIFU session with two‑to‑three visits per patient per year can typically recover device cost in 6–18 months, depending on utilization, financing, and whether the base unit is new or certified pre‑owned. ALLWILL regularly advises clinics to model scenarios at 30%, 60%, and 80% booking rates to avoid overly optimistic ROI assumptions.

Why Multi‑Depth HIFU Justifies a Higher Ticket

For a clinic that already owns RF or IPL, adopting a multi‑depth Jeisys‑type HIFU platform is a higher‑ticket decision but can be justified by several clinical and operational differentiators.

First, depth‑specific cartridges allow selective targeting of SMAS, dermis, and subcutaneous fat with a single console, enabling non‑surgical lifting and contouring indications that differ from surface‑oriented lasers or RF. For the patient, this often translates into a different conversation: fewer sessions, more structural tightening, and a non‑injectable alternative for jawline and midface concerns (while still avoiding efficacy promises).

Second, HIFU is typically characterized as having minimal consumables compared with per‑cycle cryolipolysis or per‑tip RF microneedling, provided cartridge inventory and line usage are tightly controlled. Training materials for multi‑cartridge HIFU emphasize reusing the same cartridges across multiple regions until line counts are exhausted, rather than swapping prematurely. That helps support more predictable margins for high‑value treatments while still keeping patient‑facing pricing competitive.

Third, because HIFU treatments can often be performed with basic topical anesthesia or no anesthesia, staffing can be flexible and chair time can be optimized, particularly in medspa environments where nurses or advanced aestheticians perform most sessions under medical oversight. For many clinic owners, this staffing efficiency is as important as the pure consumable math.

Cartridge Management Checklist: Multi‑Depth Facial & Body Configuration

The following practical checklist is designed for clinic directors and lead operators to standardize how D1.5–D13 mm cartridges are deployed by indication while preserving cartridge longevity. Depth‑to‑zone mappings are based on common training guidance for 7D/12D‑class HIFU systems.

Multi‑Depth HIFU Cartridge Management Checklist

  1. Standardize Depth‑by‑Zone Protocols (Facial)
    • Brow and forehead: prioritize 1.5 mm (superficial lines) and 3.0 mm (mid‑forehead), avoiding direct treatment over the orbital rim; use conservative line density.
    • Cheeks and midface: use 3.0 mm for most of the cheek and nasolabial support, with 4.5 mm only where soft tissue thickness and safety maps allow; avoid direct zygoma shots.
    • Nasolabial folds/perioral: emphasize 3.0 mm and 1.5 mm in a grid or linear pattern; reduce energy near dental implants or use protective gauze as directed in training.
    • Jawline/lower face: initiate with 4.5 mm along the mandibular border outside mapped nerve zones, followed by 3.0 mm for superficial tightening; stretch skin over bone to improve comfort and contact.
  2. Standardize Depth‑by‑Zone Protocols (Body Contouring)
    • Abdomen/flanks: begin with 13 mm in areas with sufficient pinch thickness, followed by 9 mm and 6 mm passes in descending order, avoiding ribs and iliac crest.
    • Thighs/arms: use 9 mm and 6 mm in zones with moderate fat; avoid areas with limited subcutaneous thickness or heavy vascular/nerve structures.
    • Always consult manufacturer safety diagrams or training manuals for “forbidden areas” and recommended line spacing.
  3. Define Line Counts & Energy Bands Per Cartridge
    • Establish standard ranges for lines per region (e.g., cheeks 80–120 lines per depth, jawline 60–100 lines, full abdomen 250–400 lines across depths), then adjust case‑by‑case.
    • Adopt conservative starting energies (e.g., 0.5–0.7 J equivalent settings where applicable) and titrate within manufacturer‑recommended ranges based on patient tolerance rather than maximizing from the outset.
  4. Implement Cartridge Life‑Cycle Tracking
    • Record starting and remaining line counts at the beginning and end of each treatment; many consoles show “total line” and “use line” data for each cartridge.
    • Assign each cartridge a unique ID and log date of first use, cumulative lines fired, and zones treated to anticipate replacement before failure or drift.
  5. Optimize Cartridge Rotation For Longevity
    • Rotate cartridges across similar‑indication patients (e.g., use a single 4.5 mm for all lower‑face passes until near end of life) rather than mixing multiple partially used cartridges.
    • Avoid aggressive pressure on the skin that could damage the transducer or crystal; manuals consistently advise gentle, full‑contact coupling instead of forceful compression.
  6. Operational Guardrails & Staff Training
    • Mandate pre‑treatment mapping: mark forbidden zones (around ears, above eyebrows, perioral region) before firing the first shot.
    • Require operators to use ultrasound gel generously to maintain coupling and to avoid dry‑firing, which can affect cartridge integrity and patient comfort.
    • Use sliding mode selectively and only after training; stamping mode offers more controlled line spacing for newer operators.
  7. Review & Audit Monthly
    • Compare projected vs. actual line usage and cartridge replacement intervals to refine protocol efficiency.
    • Conduct monthly device and cartridge inspections (visual casing checks, function tests) to identify early signs of wear or inconsistent energy delivery.
Also check:  Cynosure SculpSure Body Contouring for Clinical Fat Reduction

This checklist can be adapted to specific Jeisys HIFU models and comparable devices, but it should always be aligned with official manuals and local training guidance.

Compliance, Regulatory Positioning & Asset Protection

Multi‑depth HIFU devices intended for aesthetic lifting and fat reduction may hold region‑specific clearances (for example, FDA 510(k) clearances or CE marking) for particular indications, tissue depths, and body areas. However, indications and parameters vary by model, and off‑label protocols are a real compliance risk.

Clinic owners should verify, in writing, for each unit:

  • Exact model and software version.
  • Current regulatory status in their jurisdiction (e.g., cleared/approved indications, any limitations).
  • Whether treatment guides and protocols supplied by the manufacturer align with local regulations and scope of practice.

For certified pre‑owned units, asset protection hinges on documentation. Buyers should require detailed refurbishment reports, functional test logs, and evidence that cartridges and transducers have been evaluated, replaced, or certified as within expected lifespan. Manufacturer and independent manuals emphasize the importance of proper maintenance, including regular inspection, cleaning, and adherence to specified operating conditions (e.g., avoiding drops or fluid ingress).

ALLWILL’s role in this context is to help clinics source both new and certified pre‑owned HIFU units with clear traceability, condition reports, and support alignment with manufacturer guidelines, rather than acting as the regulatory authority.

Procurement Risks To Avoid + ALLWILL Expert View

There are several recurring procurement pitfalls with HIFU that directly affect both clinical performance and cartridge longevity:

  • Unverified cartridges and transducers: Non‑OEM or poorly refurbished cartridges may deliver inconsistent energy, reduce line capacity, or raise patient safety concerns. Manuals assume OEM‑spec components.
  • Missing or outdated protocols: Buying a device without current treatment guides or depth maps pushes operators toward guesswork on D1.5–D13 mm usage, increasing risk of ineffective or uncomfortable treatments.
  • Lack of service and calibration support: Without access to trained biomedical service partners, minor handpiece issues or software faults can escalate into extended downtime and reduced asset life.

ALLWILL Expert View: Building a Cartridge‑Smart HIFU Business Case
For most clinics, HIFU ROI is not determined by retail price alone but by how rigorously the team manages cartridge line counts and treatment design per indication. Treat line capacity as a metered utility: track every shot, standardize depth‑by‑zone protocols, and avoid “extra” passes that do not add clinical value. When evaluating a new versus certified pre‑owned HIFU platform, ask vendors to show historical cartridge replacement intervals and typical line utilization patterns from similar clinics. A well‑documented CPO unit with known service history, fresh or recently tested cartridges, and verified software can sometimes outperform a brand‑new device that arrives with no structured usage plan. ALLWILL’s procurement specialists often help clinics model this trade‑off, aligning device condition, warranty scope, and consumable pricing with realistic booking assumptions, so the purchase decision is grounded in data, not just headline discounts.

Frequently Asked Questions

What is the typical price range for a multi‑depth HIFU platform and cartridges?

Also check:  Which Handpieces Work with OEM and Refurbished Aesthetic Systems

Capital prices vary widely by brand, configuration, and region, but many clinics see console ranges from mid‑five‑figure to low‑six‑figure USD equivalents, with cartridges typically priced per piece in the mid‑hundreds to low‑thousands USD. Exact numbers depend on negotiation, warranty, and whether you choose new or certified pre‑owned units. Request a quote from ALLWILL to confirm current market levels for your region and model preference.

How do new and certified pre‑owned HIFU units differ in terms of ROI?

New units generally offer full manufacturer warranty and the latest software, while certified pre‑owned devices can provide lower upfront cost with carefully defined condition and service history. ROI depends on acquisition price, anticipated treatment volume, and consumable costs. Clinics should compare multi‑year cash‑flow scenarios for both options and ensure any CPO unit comes with documented testing and support.

What warranty and service coverage should I expect?

Warranty coverage varies by manufacturer and vendor but typically includes console electronics and handpiece defects for a defined period, with separate terms for cartridges and consumables. Service agreements may cover preventive maintenance, loaner devices, or discounted parts. Buyers should request written details of coverage limits, response times, and any exclusions related to third‑party cartridges or off‑label use before committing.

How can I ensure compliance when using D1.5–D13 mm cartridges?

Compliance begins with confirming that the specific device model is cleared or approved in your jurisdiction for the indications and body areas you plan to treat, and that your protocols align with manufacturer guidelines. Operators should be trained on depth‑by‑zone usage, contraindications, and nerve‑sparing maps. Clinics should maintain documentation of training, consent forms, and device maintenance logs to support regulatory and insurer expectations.

How quickly can a HIFU device pay for itself in a clinic setting?

Payback depends on your fee schedule, booking rate, and marketing strength. Clinics that consistently schedule full‑face or face‑plus‑neck protocols several times per week often reach payback within one to two years, assuming disciplined cartridge management and realistic pricing. Underutilization is the most common reason payback takes longer, which is why many buyers consult ALLWILL for market‑specific utilization benchmarks before finalizing a purchase.

References

  1. Getting Started with the 7D HIFU Machine: Complete Training FAQ
  2. How To Perform 12D MPT HIFU Treatment: Benefits, Steps & Pro Tips
  3. Advanced 4-in-1 HIFU Treatment System – Technical Manual (Scribd)
  4. Operation Manual of HIFU – Vertical System with Three Heads
  5. Classic HIFU Manual – Areton Ltd
  6. High Intensity Focused Ultrasound – IMDA Technical and Safety Overview
  7. HIFU 7D Therapeutic Manual Guide (Scribd)
  8. HIFU Treatment Protocols: Time, Depth & Pulses
  9. Mastering HIFU Beauty Equipment: A Comprehensive Usage Guide
  10. HIFU Application – Facial Treatment Protocols (Scribd)
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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.