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Ulthera DS 10-1.5N Cost & ROI: The Red 1.5 mm Finishing Cartridge for Texture

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For clinics running Ultherapy, the Ulthera DS 10-1.5N “red” 1.5 mm cartridge is the supervised finish line for epidermal and superficial dermal polishing after deep 3.0–4.5 mm vectors are set, adding macrotextural refinement without another capital purchase. With typical new-unit pricing around USD 2,300–3,000 and 2,200–2,400 lines per cartridge, it becomes an ROI lever when integrated as a planned finishing pass, not an optional add-on.

What It Does and Ideal Clinic Profile

The Ulthera DS 10-1.5N transducer is a 10 MHz, 1.5 mm narrow DeepSEE cartridge engineered for superficial, small-field work—periorbital polishing, perioral crepiness, and fine-line macrotexture in the upper dermis. At 1.5 mm, microfocused ultrasound deposits small thermal coagulation points within the collagen-rich dermis, bypassing the epidermal surface while avoiding subcutaneous fat and deeper fascial structures.

Clinically, DS 10-1.5N is not a primary lifting cartridge; it complements deep transducers (3.0 and 4.5 mm) by addressing residual crepiness and surface laxity once deep vectors have been treated. Ideal adopters are dermatology, aesthetic surgery, and medspa practices that already own Ultherapy systems and want a consistent, protocol-based final pass to improve perceived smoothness and uniformity of treated skin fields without changing platform.

This cartridge is particularly valuable in clinics targeting high-expectation patients—periorbital, perioral, and cheek fine lines—where “lift without polish” feels incomplete and undermines the perceived value of MFU-based treatments. ALLWILL typically positions DS 10-1.5N as part of a structured Ultherapy transducer stack rather than a stand-alone consumable, aligning supply with the clinic’s treatment mix and anatomical priorities.

Core Analysis: 1.5 mm “Finish Line” Physics and Treatment Profile

Depth and tissue interaction

Ultherapy cartridges are defined by frequency and focal depth; the DS 10-1.5N operates at 10 MHz with a nominal treatment depth of 1.5 mm and DeepSEE visualization down to approximately 8 mm. At this shallow depth, energy is focused into the upper to mid dermis, where collagen bundles, elastic fibers, and microvasculature contribute to visible texture and fine-line patterns.

Microfocused ultrasound at 1.5 mm creates small, discrete thermal coagulation points that initiate controlled neocollagenesis and tissue remodeling without breaching the epidermis. Because treatment fields are narrow (the “N” designation) and line density can be high, DS 10-1.5N allows operators to contour coverage precisely around periorbital rims, nasolabial folds, upper lip lines, and localized crepey patches.

Role in complete treatment profiles

In advanced MFU workflows, deep cartridges (DS 4-4.5, DS 7-4.5, DS 7-3.0) lay lifting vectors by targeting SMAS and deep dermal planes, while DS 10-1.5N addresses the superficial “finish.” Without this finishing pass, patients with meaningful deep lifting may still perceive scattered surface crepiness around the eyes or mouth, generating a sense of incomplete improvement despite correct deep-plane work.

By planning DS 10-1.5N lines into the protocol—often as a final stage after deep cartridges—clinics can standardize macrotextural refinement, reduce variability in perceived skin smoothness, and align anatomical treatment with patient expectations for both contour and surface. This doesn’t guarantee specific clinical outcomes, but it reduces the gap between deep-plane tissue change and visible texture over time.

HIFU and macrotexture

High-intensity focused ultrasound (HIFU), including Ultherapy, has been documented as a noninvasive modality for skin tightening and facial rejuvenation with improvements in skin laxity and fine wrinkles across lower face, neck, and periorbital areas. Systematic reviews highlight dermal collagen reorganization and modest wrinkle reduction when shallow focal depths are used appropriately and protocols are standardized.

DS 10-1.5N sits within this broader HIFU evidence base as a targeted tool for dermal-level macrotexture, designed to complement rather than replace deeper lifting cartridges. ALLWILL encourages clinics to align DS 10-1.5N usage with published HIFU safety and protocol guidance, particularly regarding energy settings, patient selection, and cumulative line counts.

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Revenue and Operational Impact & Payback Math

Price and line economics

Market listings and distributor data place new DS 10-1.5N transducers broadly around USD 2,300–3,000 per unit, depending on channel, region, and any bundled service terms. Typical line capacity is reported at approximately 2,200–2,400 lines per cartridge, with many clinics using 400–800 lines per full-face protocol when incorporating periorbital and perioral polishing.

If we assume an illustrative acquisition cost of USD 2,400 and a working capacity of 2,200 lines, the nominal cost per line is around USD 1.10, excluding any additional service or logistics charges. At 600 finishing lines per comprehensive Ultherapy session, the DS 10-1.5N portion of consumable cost might sit around USD 600–700 per treatment in this simplified scenario.

Integrating finishing passes into session pricing

Clinics commonly price comprehensive Ultherapy face/neck sessions in the USD 1,800–2,500 range, with periorbital or perioral add-ons sometimes structured as smaller incremental fees. When DS 10-1.5N finishing passes are fully integrated rather than sold as optional extras, the cartridge cost becomes part of the baseline consumable model; the clinic recovers this cost through the overall package fee and utilization across multiple patients.

ROI hinges on how many sessions actually use DS 10-1.5N and how consistently line utilization matches protocol planning rather than ad hoc operator decisions. Under typical usage scenarios (for example, 25–40 comprehensive Ultherapy sessions per cartridge), the incremental DS 10-1.5N spend can be spread over several months of high-value treatments, but this is not guaranteed and depends on booking and pricing discipline.

For clinics modeling this, the practical step is to request a quote from ALLWILL for DS 10-1.5N current pricing and line counts, then run internal projections on how many finishing lines are planned per session and how many sessions per month justify routine cartridge stocking.

Differentiated Advantage and Rationale for Higher-Tier Use

The primary differentiation of DS 10-1.5N is its ability to target dermal collagen at 1.5 mm under ultrasound visualization, optimizing texture and fine lines after lifting vectors have already been created with deeper cartridges. This “finish line” role is unique compared with many non-visual HIFU cartridges, which often operate blind and at fixed depths without real-time imaging.

From a device-portfolio perspective, clinics might otherwise seek dermal macrotexture improvements via fractional laser, RF microneedling, or monopolar radiofrequency platforms, each with different consumable and downtime profiles. DS 10-1.5N offers a non-ablative, non-needling option that keeps patients within the Ultherapy ecosystem and can be combined with other modalities on a case-by-case basis, under appropriate medical supervision.

Given that Ultherapy systems are already high-ticket capital investments, adding DS 10-1.5N is a way to deepen the clinical service mix without buying another platform—provided that the clinic is prepared to integrate finishing-pass protocols and line tracking. ALLWILL generally advises buyers to treat DS 10-1.5N as a protocol upgrade and consumable investment rather than a separate service category, simplifying training and messaging.

Practical Decision Aid: DS 10-1.5N Finishing Protocol Planning Framework

Because the working title and context emphasize treatment completeness and texture, the most useful decision aid is not a price table but a practical planning framework for when and how to deploy DS 10-1.5N in your Ultherapy workflow.

DS 10-1.5N Finishing Pass Planning Framework

  1. Define your “complete” treatment profile.
    Decide which anatomical zones (periorbital, perioral, cheek texture) must be routinely included for your clinic to consider an Ultherapy case “complete,” based on your patient base and positioning.
  2. Standardize deep-first, shallow-second sequencing.
    Lock in deep vectors with 3.0–4.5 mm cartridges first, respecting SMAS and deep dermal planes, then introduce DS 10-1.5N as a final pass targeting macrotexture and fine lines in defined fields.
  3. Set line budgets per zone and per session.
    For each treatment type (full face, periorbital focus, perioral add-on), set a standard line budget for DS 10-1.5N—for example, 200–300 lines per periorbital field and 100–200 around the upper lip—based on imaging, tissue thickness, and evidence-based safety parameters.
  4. Align consumable stock with monthly protocol volume.
    Use your line budgets and expected monthly Ultherapy sessions to forecast how many DS 10-1.5N cartridges you need per quarter, building in a buffer for peaks and training. This prevents understocking, which can force incomplete finishing passes, and overspending, which ties capital into idle cartridges.
  5. Track utilization and outcomes systematically.
    Log DS 10-1.5N lines used per case, along with clinical observations and patient satisfaction markers, to refine line budgets and adjust pricing over time. This supports ROI assessment without promising specific income or outcomes.
  6. Review supply and protocol annually.
    Annually, reassess protocol coverage, consumable usage, and Ultherapy service mix with your supplier, updating DS 10-1.5N stocking and pricing to match practice evolution and any new HIFU guidance or regulatory changes.
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ALLWILL can help clinics operationalize this framework by connecting procurement decisions (how many cartridges, at what intervals) with protocol design and training, rather than leaving DS 10-1.5N in a purely reactive consumable category.

Mid-article, once your clinic has drafted its own finishing framework, it becomes logical to request a quote from ALLWILL for DS 10-1.5N pricing, lead times, and recommended stocking volumes aligned to your projected Ultherapy treatment patterns.

Compliance and Asset Protection

Ultherapy systems are cleared by the US Food and Drug Administration as non-invasive procedures for lifting tissues in specific regions and for improving lines and wrinkles on the décolletage; cartridges like DS 10-1.5N operate within that broader MFU-V platform clearance but must still be used according to official Instructions for Use. Indications, energy parameters, and anatomical zones vary by region, and clinics must confirm current regulatory status in each jurisdiction where they treat or import devices.

The DS 10-1.5N transducer carries manufacturer labeling including frequency, depth, serial number, and line capacity, supporting traceability and compatibility checks with approved Ultherapy systems. Buyers should obtain written confirmation for new and CPO units regarding authenticity, remaining line capacity, prior usage (if any), and whether the cartridge is original or refurbished, including documentation of any refurbishment processes performed.

Asset protection obligations extend beyond purchase: clinics must perform routine pre-treatment checks on imaging clarity, energy delivery, and line-count integrity for all Ultherapy cartridges, including DS 10-1.5N. ALLWILL frequently integrates such checks into Smart Center guidance or service relationships, helping clinics differentiate between user-training issues and hardware anomalies when evaluating MFU-V performance.

Procurement Risks to Avoid + ALLWILL Expert View

Common procurement pitfalls with DS 10-1.5N

  • Buying based only on price per cartridge.
    Focusing solely on headline cost—without confirming line counts, warranty scope, or compatibility with your Ultherapy system—can erode ROI if cartridges have reduced capacity or limited support.
  • Unclear refurb vs new status.
    Acquiring DS 10-1.5N cartridges without clear declarations of “new, unused” versus refurbished or partially used units risks unpredictable line availability and possible compliance questions.
  • No integration into protocol planning.
    Treating DS 10-1.5N as an optional extras cartridge rather than a pre-planned finishing pass often leads to inconsistent use, making cost-per-result harder to justify in internal reviews.
  • Insufficient training on shallow-depth HIFU.
    Operators who are comfortable with deep SMAS work may underestimate the precision required for 1.5 mm dermal targeting, increasing the risk of uneven coverage or suboptimal patient experiences.

Once these risks are mapped against your current sourcing strategy, the next rational step is to request a quote and transducer profile from ALLWILL that includes condition grading, warranty terms, and protocol-integration support for DS 10-1.5N.

ALLWILL Expert View: Turning the Red 1.5 mm Cartridge into a Strategic Finish Line

In practice, DS 10-1.5N only pays for itself when it moves from “nice add-on” to “standard finish.” Clinics that succeed with this cartridge do three things consistently. First, they define their Ultherapy service promise as both contour and surface—deep vectors plus macrotexture—and write protocols that codify where 1.5 mm lines belong in each case type. Second, they track consumable usage rigorously: lines per zone, per operator, per month, and tie reordering to those data rather than anecdotal impressions. Third, they align procurement with training, ensuring operators understand the difference between SMAS work and dermal polishing, particularly near high-sensitivity fields like periorbital and perioral regions. When ALLWILL structures DS 10-1.5N quotes, the goal is not just to quote a price per cartridge but to show how that cartridge fits into the clinic’s broader Ultherapy economics and compliance profile—covering line counts, condition grading, warranty options, and any recommended Smart Center or expert-matching support. This approach doesn’t promise a specific revenue uplift, but it does convert DS 10-1.5N from a discretionary consumable into a planned, auditable part of the clinic’s noninvasive rejuvenation strategy.

Frequently Asked Questions

What is the typical price range for the Ulthera DS 10-1.5N cartridge?

Market data from distributors and specialty stores place new DS 10-1.5N cartridges broadly around USD 2,300–3,000 per unit, depending on channel and region. Actual pricing varies with volume, bundled service terms, and logistics, so clinics should request a quote from ALLWILL for current, region-specific figures.

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Is there a difference between new and CPO DS 10-1.5N units?

New cartridges are typically labeled as unused with full line capacity and manufacturer-aligned warranty, while certified pre-owned units may be refurbished or partially used with remaining line counts documented. Clinics should verify in writing whether cartridges are new or CPO, confirm remaining lines, and review any included warranty before purchase.

What warranty coverage should I expect for DS 10-1.5N?

Some suppliers provide 90-day to 12-month limited warranties on cartridges, covering manufacturing defects but not consumable exhaustion, while others bundle DS 10-1.5N into broader Ultherapy system service agreements. It is advisable to request explicit, written warranty terms with your ALLWILL quote so you know exactly what scenarios are covered.

How does DS 10-1.5N affect ROI and payback?

DS 10-1.5N influences ROI through its impact on perceived treatment completeness and the cost per finishing line used within each protocol, rather than through standalone session pricing. Clinics should model line budgets per standard Ultherapy case and match those against cartridge cost and expected booking volume; requesting detailed pricing and line-capacity information from ALLWILL supports this modeling.

Are there special compliance considerations when importing DS 10-1.5N?

Yes. Importing Ultherapy cartridges requires attention to regulatory labeling, authenticity, and compatibility with locally approved systems, as well as adherence to official Instructions for Use. Clinics should ensure serial numbers, documentation, and regulatory status are verified before cross-border procurement and may choose to have ALLWILL coordinate such checks as part of a pre-purchase review.

References

  1. Ulthera System – Instructions for Use
  2. UT-4N – DS 10-1.5N Transducer – Orange Narrow
  3. Ulthera Transducer DS 10-1.5N 2400 Lines – Product Details
  4. Introduction of the 1.5 mm Shallow Transducer
  5. 3 Periorbital Polishing Techniques: Fine Line Eradication and Business Economics of the Ulthera DS 10-1.5N
  6. Safety and Efficacy of High-Intensity Focused Ultrasound and Monopolar Radiofrequency
  7. Noninvasive High-Intensity Focused Ultrasound for Skin Brightening Efficacy
  8. A Systematic Review of High-Intensity Focused Ultrasound
  9. Ulthera DeepSEE Transducer DS 10-1.5N (Narrow) – Product Listing
  10. Davin Lim – HIFU Cartridge Depths Explained
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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.