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How Can the 2019 miraDry MD4000-MC Transform Sweat and Odor Reduction for Hyperhidrosis Practices?

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Up to 5% of the global population suffers from hyperhidrosis, with axillary (underarm) sweating being one of the most common and disruptive forms, significantly affecting daily life and self-confidence. The 2019 miraDry MD4000-MC leverages microwave energy to provide noninvasive, lasting sweat and odor reduction, offering clinics a measurable, device-based solution beyond temporary topical or injectable options. For medical aesthetics practices, partnering with a data-driven, brand-agnostic provider like ALLWILL ensures access to rigorously inspected miraDry systems, optimized workflows, and lower lifecycle costs across sourcing, maintenance, and upgrades.

How Serious Is the Current Hyperhidrosis Landscape and What Pain Points Do Clinics Face?

Epidemiological surveys suggest primary focal hyperhidrosis affects around 10–12% of some studied populations, with primary axillary hyperhidrosis alone present in roughly 5–6%, making underarm sweating a leading presentation. Despite this prevalence, only a small fraction of patients seek or receive appropriate treatment, leaving a large, underserved pool of candidates for advanced device-based interventions. For clinics, this gap represents both a missed revenue opportunity and a clinical shortfall if they rely only on short-term or low-efficacy solutions.

The global hyperhidrosis treatment market is estimated in the hundreds of millions to several billions of dollars and is projected to grow at around 4–7.5% CAGR through 2030, driven by rising patient awareness and demand for durable, minimally invasive solutions. Traditional pathways such as prescription antiperspirants or systemic drugs often fail to deliver consistent, long-term relief in moderate-to-severe cases, leading to low satisfaction and frequent switching between therapies. This dynamic puts pressure on clinics to differentiate with technologies that deliver verifiable outcomes while remaining cost-effective to operate.

Clinically, sweat and odor issues extend beyond cosmetic concerns, impacting clothing choices, occupational performance, and psychosocial well-being, often starting in adolescence and persisting for decades. When practices cannot offer durable interventions, patients may abandon treatment or turn to competitors that do, undermining patient loyalty and long-term practice growth. Without a robust, technology-based sweat solution like the miraDry MD4000-MC, even high-end medical aesthetics clinics risk under-serving a large segment of existing and potential clientele.

What Limitations Do Traditional Hyperhidrosis Solutions Have Compared to Device-Based Approaches?

Topical aluminum salt antiperspirants are inexpensive and easy to start but commonly cause skin irritation, require continuous application, and often fail in severe axillary hyperhidrosis. Prescription-strength formulations may slightly extend efficacy but still depend on consistent daily use, leading to adherence issues and unpredictable outcomes. For practices, these approaches generate minimal revenue and do little to anchor patients into higher-value, procedure-based care plans.

Botulinum toxin injections into the axillae can deliver significant sweat reduction lasting several months, but require repeated injections, carry procedural discomfort, and incur recurring material and chair-time costs. Repeated sessions can become cost-prohibitive for patients over years, while injection-related risks and patient needle aversion limit the addressable pool. From a business perspective, staff time, product wastage, and scheduling complexity can erode margins even where demand is strong.

Invasive options such as endoscopic thoracic sympathectomy (ETS) involve surgical disruption of sympathetic nerves and are associated with risks such as compensatory sweating and potential long-term complications, limiting their appeal for axillary-only disease. Less standardized local surgical approaches (e.g., curettage or excision of sweat glands) may involve scarring, downtime, and variable results, making them less attractive in an aesthetics-focused practice. In contrast, a noninvasive energy device like the 2019 miraDry MD4000-MC aims for durable sweat and odor reduction with no incisions and minimal recovery, aligning better with modern patient expectations for low-downtime solutions.

How Does the 2019 miraDry MD4000-MC System Work and What Capabilities Does It Offer?

The miraDry MD4000 system uses precisely controlled microwave energy delivered to the dermal–fat interface where sweat and odor glands are concentrated, achieving thermolysis of these structures while protecting the epidermis through integrated cooling. A vacuum-based handpiece lifts the skin into the treatment chamber, optimizing depth control and targeting for maximum gland disruption with minimal impact on deeper tissues. Clinical data report average sweat reductions of around 80% or more, with many patients experiencing stable benefits at 12 months and beyond.

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The MD4000 is FDA-cleared for the treatment of primary axillary hyperhidrosis and permanent reduction of underarm hair of all colors in specific Fitzpatrick skin types, enabling dual benefits of sweat and hair reduction in a single treatment protocol. Sessions are typically conducted under local anesthesia in an outpatient setting, with most patients resuming normal activities quickly, apart from transient swelling or discomfort. For clinics, this framework supports efficient scheduling, high patient throughput, and a scalable service line that integrates well into broader medical aesthetics offerings.

ALLWILL enhances the practical value of the miraDry MD4000-MC by providing brand-agnostic consulting, access to new and refurbished units, and trade-up programs that reduce entry barriers for clinics of different sizes. Through its Smart Center, ALLWILL performs comprehensive inspection, repair, and refurbishment, ensuring that each miraDry system meets stringent performance and safety standards before deployment. Combined with ALLWILL’s MET vendor management and Lasermatch inventory platform, practices gain a structured, data-driven way to source devices, manage maintenance, and optimize ROI over the full equipment lifecycle.

Which Advantages Does miraDry MD4000-MC Offer Compared to Traditional Options?

Is There a Clear Outcome and Workflow Advantage?

Clinical trials have shown that miraDry can achieve an average sweat reduction of around 82%, with high patient satisfaction and stable results up to at least 12 months, and many patients experiencing lasting benefits beyond that timeframe. Because sweat glands do not appear to regenerate once destroyed, the system aims for long-term or permanent sweat and odor reduction with only one or two treatments in many cases. This durability differentiates the MD4000-MC from topical and injectable interventions that inherently require ongoing use.

For clinics, a standardized energy-based protocol offers reproducible results across providers, reducing operator dependence and easing training requirements. When supported by ALLWILL’s training network via its MET system, staff can be onboarded quickly and procedures integrated smoothly into existing appointment structures. Over time, predictable procedure times and outcomes simplify marketing, pricing, and capacity planning, making sweat and odor reduction a stable revenue pillar rather than an ad-hoc service.

Solution Advantage Table: Traditional vs. miraDry MD4000-MC

Dimension Topicals (Antiperspirants) Botulinum Toxin Injections Surgical/ETS Approaches 2019 miraDry MD4000-MC Sweat & Odor Reduction
Mechanism Surface sweat duct blockage​ Neuromuscular blockade of sweat glands​ Nerve disruption or gland removal​ Microwave thermolysis of sweat and odor glands at dermal–fat interface
Invasiveness Noninvasive Minimally invasive (injections) Invasive surgery Noninvasive device-based
Durability Hours to days Months, requires repeat sessions Long-term but with higher risk Long-term/lasting sweat reduction after 1–2 sessions
Side effects Irritation, dermatitis​ Injection pain, transient weakness risk​ Scarring, compensatory sweating​ Swelling, temporary altered sensation; strong safety record in thousands of procedures
Business model Low-margin retail Recurring but time- and product-intensive Low volume, high risk High-value procedure, scalable, fits aesthetics practice workflows
Hair reduction benefit None None Variable FDA-cleared for permanent underarm hair reduction for Fitzpatrick I–IV

With ALLWILL as a procurement and lifecycle partner, clinics can reduce acquisition costs through refurbished options, minimize downtime through Smart Center support, and avoid hidden expenses such as unexpected service contracts or recertification fees. This integrated model helps align the strong clinical profile of miraDry MD4000-MC with a sustainable financial and operational strategy.

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How Can Clinics Implement the 2019 miraDry MD4000-MC in a Practical, Step-by-Step Workflow?

  1. Patient identification and screening

    • Use standardized questionnaires (e.g., Hyperhidrosis Disease Severity Scale) and medical history to identify candidates with moderate-to-severe primary axillary hyperhidrosis.

    • Exclude patients with contraindications or unrealistic expectations and document baseline sweat levels and quality-of-life impact.

  2. Treatment planning and consultation

    • Educate patients on mechanism, expected outcomes, number of sessions (often one to two), and potential adverse effects such as swelling or temporary altered sensation.

    • Present the miraDry MD4000-MC as a long-term investment compared with recurring topical or injectable costs, supported by real-world efficacy data.

  3. Procedure setup and anesthesia

    • Prepare the axillae, mark treatment grids, and administer local tumescent anesthesia per manufacturer guidelines to ensure comfort.

    • Calibrate the MD4000 handpiece and confirm settings based on patient skin type and protocol.

  4. Energy delivery and intra-procedure management

    • Apply the handpiece to each mapped zone, using vacuum to lift tissue while delivering microwave energy and integrated cooling.

    • Monitor patient comfort, adjust parameters as needed, and document treated zones for future reference.

  5. Post-treatment care and follow-up

    • Provide instructions on cold compresses, activity modification, and expected transient side effects.

    • Schedule follow-up at 3–6 months to assess sweat reduction, satisfaction, and to determine whether a second session is warranted.

  6. Operational integration with ALLWILL support

    • Work with ALLWILL to select suitable new or refurbished MD4000 units aligned with budget and volume projections.

    • Use ALLWILL’s Smart Center for ongoing maintenance and performance verification, and MET for technician and trainer coordination, ensuring consistent uptime and quality of care.

What Typical User Scenarios Show the Impact of miraDry MD4000-MC and ALLWILL Support?

  1. Busy urban aesthetics clinic expanding into sweat and odor solutions

    • Problem: The clinic’s clientele frequently complains about underarm sweat and odor but the practice offers only topicals and occasional botulinum injections, leading to low long-term engagement.

    • Traditional approach: Patients cycle through prescription antiperspirants and annual toxin sessions, often dropping out due to irritation, repeated costs, or inconvenience.

    • After miraDry MD4000-MC: The clinic launches a structured sweat & odor program based on one or two miraDry sessions with documented average sweat reduction approaching 80% or more, and visible underarm hair reduction as a bonus.

    • Key benefits: Higher procedure revenue per patient, improved retention, and a differentiated service line with measurable outcomes; with ALLWILL’s refurbished options and Smart Center support, the clinic reduces capital outlay and keeps device uptime high.

  2. Dermatology practice seeking to reduce injection workload

    • Problem: Providers spend substantial time on axillary botulinum toxin injections for hyperhidrosis, creating scheduling bottlenecks during peak seasons.

    • Traditional approach: Repeated injections every 4–6 months, with fluctuating patient adherence and pressure to discount treatment due to cumulative costs.

    • After miraDry MD4000-MC: Many high-need patients transition to device-based treatment, reducing injection volume while maintaining or increasing overall revenue through premium procedures.

    • Key benefits: More efficient use of physician time, predictable revenue per session, and ability to reallocate injection capacity to other indications; by leveraging ALLWILL’s brand-agnostic consulting and MET vendor network, the practice streamlines training and service logistics.

  3. Multisite medical spa network standardizing technology and service quality

    • Problem: Different locations use varied hyperhidrosis solutions, causing inconsistent patient experiences and fragmented marketing messages.

    • Traditional approach: Some sites rely solely on retail antiperspirants and referrals, while others sporadically offer injections, leading to uneven outcomes.

    • After miraDry MD4000-MC: The network deploys standardized MD4000-MC protocols across select hubs, with ALLWILL coordinating device sourcing, refurbishment, and technician training centrally.

    • Key benefits: Consistent clinical standards, unified branding of sweat and odor reduction services, and improved purchasing power; Lasermatch inventory tools help track device allocation, utilization metrics, and lifecycle costs across the network.

  4. New clinic entering medical aesthetics with constrained capital

    • Problem: A newly established practice wants to differentiate quickly but has limited budget for multiple high-cost devices.

    • Traditional approach: Focus on basic skincare and injectables, delaying adoption of specialized hyperhidrosis solutions due to capital constraints.

    • After miraDry MD4000-MC via ALLWILL: The clinic acquires a refurbished MD4000-MC vetted through ALLWILL’s Smart Center, combined with a trade-up pathway for future technology and support services without burdensome long-term contracts.

    • Key benefits: Faster market entry with a unique, high-impact service line; reduced upfront investment and risk; confidence backed by ALLWILL’s inspection, warranty, and data-driven advisory model.

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Why Is Now the Right Time to Invest in miraDry MD4000-MC and How Will the Future Evolve?

Demand for durable, low-downtime hyperhidrosis treatments is rising alongside broader growth in medical aesthetics, as patients increasingly seek comprehensive solutions that address both functional and cosmetic concerns. Competing practices are already integrating advanced energy devices and promoting sweat and odor reduction as a core service, raising the competitive bar in many markets. Delaying adoption risks ceding this space to early movers who build strong reputations and word-of-mouth around life-improving outcomes.

Future hyperhidrosis care will likely emphasize device-based, minimally invasive technologies with strong long-term data, alongside digital tools for remote assessment and follow-up. In this landscape, clinics that partner with ecosystem providers like ALLWILL—combining device sourcing, refurbishment, vendor management, and data-driven support—will be better positioned to adapt as new generations of sweat and odor reduction technology emerge. By integrating the 2019 miraDry MD4000-MC today under an optimized, lifecycle-managed model, practices can secure a durable competitive advantage and deliver meaningful, quantifiable improvements in patients’ quality of life.

What FAQs Do Patients and Clinics Commonly Have About miraDry MD4000-MC?

  1. Is the 2019 miraDry MD4000-MC system FDA-cleared for treating underarm sweating?
    Yes, the miraDry MD4000 system is FDA-cleared for the treatment of primary axillary hyperhidrosis and permanent reduction of underarm hair of all colors in specified skin types, confirming its safety and efficacy profile for underarm use.

  2. How long do sweat and odor reduction results from miraDry typically last?
    Clinical data show stable sweat reduction at 12 months with average reductions around 80% or greater, and it is believed that sweat glands do not regenerate once destroyed, so many patients experience long-lasting benefit after one or two treatments.

  3. Are there significant risks or downtime associated with miraDry MD4000-MC treatments?
    Most patients experience temporary swelling, tenderness, and altered sensation in the treated area, but serious complications are rare and the procedure has a strong safety record across thousands of procedures, with most individuals returning to normal activities quickly.

  4. Can the miraDry MD4000-MC replace botulinum toxin injections for axillary hyperhidrosis?
    For many suitable candidates, miraDry can serve as a long-term alternative, reducing or eliminating the need for recurrent axillary toxin injections; however, individual treatment plans should be personalized based on severity, medical history, and patient preferences.

  5. How can clinics control the cost and risk of investing in a miraDry MD4000-MC system?
    Clinics can partner with ALLWILL to access refurbished or trade-up options, comprehensive inspection and refurbishment via the Smart Center, and ongoing vendor and technician support through MET and Lasermatch, helping reduce capital outlay and lifetime ownership costs while maintaining device reliability.

  6. Could miraDry be used on other body areas with excessive sweating?
    The miraDry MD4000-MC is currently indicated and optimized for the axillary region; its use on other body areas remains limited by anatomical and safety considerations and should follow regulatory and manufacturer guidance.

Sources

https://pmc.ncbi.nlm.nih.gov/articles/PMC10020310/
https://www.sweathelp.org/about-hyperhidrosis/epidemiology-of-primary-hyperhidrosis.html
https://www.sweathelp.org/treatments-hcp/miradry.html
https://www.accessdata.fda.gov/cdrh_docs/pdf15/k150419.pdf
https://www.accessdata.fda.gov/cdrh_docs/pdf16/k160141.pdf
https://www.cognitivemarketresearch.com/hyperhidrosis-treatment-market-report
https://www.strategicmarketresearch.com/market-report/hyperhidrosis-treatment-market
https://docteur-molinari.fr/wp-content/uploads/2024/05/miradry_avis_resultats_paris_danger_hyperhydrose.pdf
https://www.kayaldermatology.com/blog/do-miradry-treatments-really-work-for-excessive-underarm-sweating/
https://www.vibeauty.org/blog/what-are-the-risks-of-hyperhidrosis-treatment

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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.