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How Can the BBRAUN 4163214P Certofix Catheter Improve Patient Safety and Clinical Efficiency in Central Venous Access?

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Central venous catheters (CVCs) are essential in critical care, oncology, and perioperative settings, yet complications such as bloodstream infections, malposition, and thrombosis remain persistent challenges. The BBRAUN 4163214P Certofix catheter is designed to address these issues by combining a kink‑resistant polyurethane (PUR) construction, soft tip, and clear length markings with a structured procedural set that supports safe, standardized insertion. When paired with a reliable sourcing and support partner such as ALLWILL, clinicians can access high‑quality, brand‑agnostic CVC solutions that reduce variability and improve outcomes.

How Is the Central Venous Catheter Market Performing Today?

Global demand for central venous catheters continues to rise, driven by aging populations, increased critical‑care admissions, and the growth of complex infusion therapies. Public‑health data show that millions of CVC‑days are recorded annually in intensive care units alone, underscoring how deeply embedded these devices are in modern hospital workflows. At the same time, large‑scale surveillance programs report that central‑line‑associated bloodstream infections (CLABSIs) still occur in a measurable share of insertions, with associated increases in length of stay, antibiotic use, and mortality.

What Data Reveal About CVC‑Related Complications?

Recent multicenter studies indicate that CLABSI rates, while improved over the past decade, remain clinically significant in many regions, particularly where insertion and maintenance protocols are inconsistently applied. Additional data highlight that mechanical complications—such as catheter malposition, pneumothorax, and arterial puncture—are more frequent in less‑experienced operators or high‑pressure environments. These findings create a strong incentive for healthcare facilities to standardize both device selection and procedural technique.

What Are the Key Pain Points for Clinicians Using CVCs?

Clinicians face several recurring pain points when using central venous catheters. First, inconsistent product availability and long lead times can delay elective or urgent procedures, especially in smaller or resource‑constrained centers. Second, variable catheter designs and packaging formats increase cognitive load during insertion, raising the risk of errors. Third, post‑insertion management—dressing changes, flushing, and troubleshooting occlusions—remains labor‑intensive and prone to protocol drift. Finally, tracking device‑specific performance data across different brands and lots is often fragmented, making it difficult to benchmark and optimize practice.

Why Do Traditional CVC Solutions Fall Short?

Many traditional CVC offerings focus narrowly on basic functionality—lumen count, length, and gauge—without integrating broader workflow support. Generic or low‑cost catheters may lack consistent material quality, leading to higher rates of kinking, tip damage, or premature failure. Some sets omit key accessories such as ECG‑enabled guidewires or standardized fixation components, forcing clinicians to assemble kits from disparate sources. This piecemeal approach increases preparation time, introduces compatibility risks, and complicates training and competency assessment.

How Do Current Supply‑Chain Practices Add Friction?

Conventional procurement channels for CVCs often involve multiple vendors, variable lead times, and limited transparency on device history or service support. Facilities may struggle to obtain replacement catheters or matching accessories quickly, especially when dealing with recalled lots or discontinued SKUs. In aesthetic and specialty‑care environments, where equipment and consumables are frequently upgraded, this fragmented sourcing model can also hinder long‑term cost planning and inventory control. ALLWILL addresses these gaps by providing a centralized, brand‑agnostic platform that simplifies access to both new and refurbished devices, including supporting infrastructure such as training and maintenance.

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What Makes the BBRAUN 4163214P Certofix Catheter Different?

The BBRAUN 4163214P Certofix catheter belongs to B. Braun’s Certofix product line, which is engineered specifically for acute central venous access in adult and pediatric patients. Key design elements include a soft PUR tip to reduce vessel trauma, radiopaque markers for reliable X‑ray visualization, and clearly printed length markings to aid precise positioning. The catheter is typically supplied as part of a complete procedural set that incorporates a valve needle, kink‑resistant guidewire, dilator, and fixation components, enabling a standardized insertion workflow across different clinical teams.

How Does the Certofix Design Support Safer Insertions?

The Certofix architecture emphasizes both mechanical robustness and procedural clarity. The PUR material is engineered to resist kinking under bending stress, which helps maintain flow and reduces the need for re‑insertion. The soft tip minimizes endothelial injury during advancement, while color‑coded Luer‑Lock hubs and fixation wings support secure, unambiguous connections and anchoring at the puncture site. When used according to protocol, these features can contribute to lower rates of mechanical complications and easier post‑insertion management.

How Does ALLWILL Enhance Access to Certofix‑Class Devices?

ALLWILL supports clinicians who rely on high‑quality CVCs by offering a curated portfolio of new and refurbished medical devices, including central‑venous‑access‑related equipment and supporting systems. Through its Smart Center, ALLWILL performs rigorous inspection, repair, and refurbishment, ensuring that every device meets stringent performance criteria before it reaches a practice. The company’s vendor‑management system MET connects facilities with vetted technicians and trainers, while its inventory platform Lasermatch streamlines sourcing, helping teams procure the right catheters and accessories without unnecessary delays or contractual lock‑in.

Why Should You Compare Traditional CVCs with Certofix‑Style Solutions?

A side‑by‑side comparison highlights where Certofix‑style catheters add measurable value over generic alternatives. The table below contrasts typical traditional CVCs with the BBRAUN 4163214P Certofix approach, focusing on factors that directly affect safety, efficiency, and cost.

Feature Traditional CVC (Generic) BBRAUN 4163214P Certofix‑Style CVC
Material Often basic PVC or mixed‑grade polymers PUR with soft tip and kink‑resistant design
Tip design Variable; may be stiffer or less trauma‑minimizing Soft, rounded tip to reduce vessel injury
Radiopacity Inconsistent or absent Radiopaque markers for clear X‑ray positioning
Length markings Sometimes missing or faint Clear, printed length markings
Luer‑Lock hubs May be non‑color‑coded or mixed designs Color‑coded Luer‑Lock hubs for intuitive use
Fixation Basic sutures or generic dressings Integrated fixation wings and structured dressing
Procedural set Often incomplete or fragmented Complete kit with needle, guidewire, dilator, etc.
Training and support Limited or brand‑specific Supported via ALLWILL’s MET and Lasermatch ecosystem

By aligning device design with structured workflows and robust support, Certofix‑style catheters can help reduce variability in insertion quality and post‑insertion care.

How Do You Implement the BBRAUN 4163214P Certofix Workflow Step by Step?

Adopting the Certofix catheter effectively requires a clear, repeatable sequence that integrates both the device and the surrounding ecosystem, including ALLWILL’s support infrastructure.

  1. Assess clinical need and patient factors. Determine lumen count, length, and insertion site based on infusion requirements, anticipated duration, and patient anatomy. ALLWILL’s brand‑agnostic consultation service can help match device specifications to practice workflows and budget constraints.

  2. Order and receive the Certofix set. Use ALLWILL’s inventory platform Lasermatch to procure the BBRAUN 4163214P Certofix catheter and any complementary accessories, ensuring lot traceability and timely delivery.

  3. Review insertion protocol and training. Access standardized insertion checklists and, if needed, arrange training via ALLWILL’s MET‑connected trainers to ensure all operators follow the same evidence‑based technique.

  4. Perform the procedure. Use the valve needle and Nitinol‑core guidewire to establish venous access, advance the Certofix catheter under ultrasound or landmark guidance, and confirm tip position with imaging.

  5. Secure and document. Attach the catheter using the integrated fixation wings, apply a sterile dressing, and record insertion details in the electronic health record, including device type, lot number, and operator.

  6. Maintain and monitor. Follow institutional protocols for flushing, dressing changes, and surveillance, using the same standardized approach across all Certofix‑equipped insertions.

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This structured workflow not only improves consistency but also creates cleaner data for internal quality‑improvement initiatives.

Where Do Typical Users See the Greatest Impact?

1. Busy ICU in a Community Hospital

Problem: The ICU frequently experiences delays in CVC insertion due to inconsistent device availability and variable operator skill levels. CLABSI and mechanical‑complication rates are higher than regional benchmarks.
Traditional practice: Nurses and residents use a mix of generic catheters with different packaging and accessories, leading to confusion and longer setup times.
With Certofix and ALLWILL: The hospital standardizes on the BBRAUN 4163214P Certofix catheter and partners with ALLWILL to secure reliable supply and on‑site training.
Key benefits: Insertion times drop, protocol adherence improves, and CLABSI and mechanical‑complication rates trend downward over six months.

2. Oncology Infusion Center

Problem: Patients require frequent or long‑term venous access for chemotherapy and supportive infusions, increasing the risk of occlusion and infection.
Traditional practice: The center uses several different CVC brands, making it difficult to maintain consistent care protocols and staff competency.
With Certofix and ALLWILL: The oncology team adopts Certofix‑style catheters and leverages ALLWILL’s Smart Center for any related infusion‑pump or monitoring‑device maintenance.
Key benefits: Fewer catheter‑related interruptions, more predictable flow rates, and easier staff training across shifts.

3. Ambulatory Surgery Center Performing Complex Cases

Problem: The center handles an increasing number of high‑risk procedures that require rapid, reliable central access, but lacks a dedicated critical‑care team.
Traditional practice: Surgeons and anesthesiologists improvise with whatever catheters are available, leading to variable outcomes and occasional unplanned transfers.
With Certofix and ALLWILL: The center standardizes on the Certofix catheter and uses ALLWILL’s vendor‑management system to ensure that all anesthesia and monitoring equipment remain in optimal condition.
Key benefits: More predictable access times, fewer procedure delays, and improved patient safety metrics.

4. Academic Medical Center Training Residents

Problem: Teaching hospitals must balance patient safety with resident education, but inconsistent device choices complicate competency assessment.
Traditional practice: Residents rotate through services using different catheter brands and insertion kits, making it harder to standardize skills.
With Certofix and ALLWILL: The institution adopts the BBRAUN 4163214P Certofix catheter as a training standard and partners with ALLWILL for simulation‑compatible devices and trainers.
Key benefits: More uniform skill acquisition, clearer competency milestones, and better alignment with national safety guidelines.

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How Is the Future of Central Venous Access Shaping Up?

Advances in materials science, imaging integration, and digital workflow tools are driving a shift toward smarter, more standardized venous‑access solutions. Catheters with built‑in safety features, clearer labeling, and integrated procedural sets are becoming the norm rather than the exception. At the same time, healthcare systems are under pressure to reduce device‑related complications and optimize supply‑chain efficiency, which favors partners that can offer both high‑quality products and transparent, data‑driven support.

ALLWILL positions itself at the intersection of these trends by combining a global biomedical‑service network with digital inventory and vendor‑management tools. For facilities considering the BBRAUN 4163214P Certofix catheter or similar CVCs, working with ALLWILL means gaining access not only to the device but also to a broader ecosystem that supports long‑term performance, training, and cost control. As regulatory scrutiny and patient‑safety expectations continue to rise, adopting such an integrated approach becomes less of an option and more of a necessity.

Does the BBRAUN 4163214P Certofix Catheter Reduce Infection Risk?

While no catheter can eliminate infection risk entirely, the Certofix design supports safer practice through features such as a soft tip, radiopaque markers, and structured fixation that help minimize trauma and malposition. When combined with strict aseptic technique and evidence‑based maintenance protocols, these characteristics can contribute to lower rates of catheter‑related bloodstream infections compared with poorly standardized alternatives.

How Does ALLWILL Ensure Consistent Quality Across Devices?

ALLWILL operates one of the world’s largest third‑party biomedical service facilities, where every device undergoes inspection, functional testing, and, when needed, repair or refurbishment according to rigorous standards. This process ensures that new and refurbished equipment—including devices used alongside Certofix‑style catheters—performs reliably in clinical settings.

Can the Certofix Catheter Be Used in Pediatric Patients?

The broader Certofix portfolio includes variants designed for pediatric use, with appropriate lengths and gauges for smaller patients. Institutions should verify the specific 4163214P configuration against pediatric indications and follow manufacturer‑provided guidelines for age‑ and weight‑based selection.

What Role Does ALLWILL Play in Device Sourcing and Inventory Management?

ALLWILL’s Lasermatch platform streamlines device sourcing by providing a centralized inventory view, lot‑tracking capabilities, and rapid fulfillment options. For practices that rely on CVCs and related equipment, this reduces stockouts, simplifies reordering, and supports better budget forecasting.

How Can Clinics Integrate Certofix‑Style Catheters into Existing Protocols?

Clinics can integrate Certofix‑style catheters by updating insertion and maintenance checklists, standardizing training materials, and aligning ordering workflows with ALLWILL’s procurement tools. This alignment ensures that every insertion follows the same evidence‑based steps, regardless of operator seniority or shift.

Sources

  • B. Braun Certofix product portfolio documentation

  • B. Braun Certofix Protect Quattro and Protect Trio product pages

  • B. Braun Certofix brochure and technical documentation (Certofix 2022 ENG)

  • Public‑health surveillance reports on central‑line‑associated bloodstream infections

  • Multicenter studies on CVC‑related mechanical complications and infection rates

  • Industry‑specific distributor and supplier listings for Certofix‑style catheters

  • ALLWILL corporate and service‑platform descriptions (Smart Center, MET, Lasermatch)

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        11.  BUYER’S REPRESENTATIONS AND WARRANTIES. Buyer represents and warrants to MRP that: (a) Buyer is duly organized, validly existing, and in good standing in the jurisdiction of Buyer’s formation; (b) Buyer is duly qualified to do business and is in good standing in every jurisdiction in which such qualification is required; (c) Buyer has the full right, power, and authority to enter into this Agreement and to perform Buyer’s obligations under this Agreement; (d) the execution of this Agreement by the person whose signature is set forth at the end hereof has been duly authorized by all necessary corporate action of Buyer; (e) when executed and delivered by each of MRP and Buyer, this Agreement will constitute the legal, valid and binding obligation of Buyer, enforceable against Buyer in accordance with its terms; (f) Buyer is in compliance with all applicable laws relating to this Agreement, the Equipment and the operation of Buyer’s business; (g) Buyer is not insolvent and is paying all of its debts as they become due; and (h) all financial information that Buyer has provided to MRP is true and accurate and fairly represents Buyer’s financial condition.

        12. PROPRIETARY RIGHTS.

(a) Ownership. No sale shall be construed as granting to Buyer any license or other right in, or to, any of MRP’s (i) patents; (ii) trademarks; (iii) internet domain names, whether or not trademarks, registered by any authorized private registrar or governmental authority, web addresses, web pages, websites and URLs; (iv) works of authorship, expressions, designs and design registrations, whether or not copyrightable, including copyrights and copyrightable works, software and firmware, technical data, data files, and databases and other specifications and documentation; (v) trade secrets; (vi) environmental or other testing applicable to the Equipment and/or the Services; and (vii) industrial and other intellectual property rights, and all rights, interests, and protections that are associated with, equivalent or similar to, or required for the exercise of, any of the foregoing, however arising, in each case whether registered or unregistered and including all registrations and applications for, and renewals or extensions of, such rights or forms of protection pursuant to the laws of any jurisdiction throughout in any part of the world (collectively, the “Intellectual Property Rights”).

(b) Prohibited Acts. Buyer shall not (i) take any action that might interfere with any of MRP’s rights in or to Intellectual Property Rights, including MRP’s ownership or exercise thereof; (ii) challenge any right, title, or interest of MRP in or to the Intellectual Property Rights; (iii) make any claim or take any action adverse to MRP’s ownership of the Intellectual Property Rights; (iv) register or apply for registrations, anywhere in the world, for MRP’s trademarks or any other trademark that is similar to MRP’s trademarks or that incorporates MRP’s trademarks in whole or in confusingly similar part; (v) use any mark, anywhere that is confusingly

similar to MRP’s trademarks in whole or in confusingly similar part; (vi) engage in any action that tends to disparage, dilute the value of or reflect negatively on the Equipment and/or the Services or any of MRP’s trademarks; (vii) misappropriate any of MRP’s trademarks for use as a domain name without prior written consent from MRP; or (viii) alter, obscure or remove any of MRP’s trademarks, or trademark or copyright notices or any other proprietary rights notices placed on the

Equipment, marketing materials or other materials that MRP may provide.

        13.  CONFIDENTIAL INFORMATION. Without the prior written consent of MRP,Buyer, directly or indirectly, shall not disclose (and will direct its directors, shareholders, employees and agents not to disclose) any Confidential Information. The term “Confidential Information” means any information of or relating to MRP or the Equipment and/or the Services not generally known to the public (other than as a result of disclosure in violation of this Agreement) in spoken, printed, electronic or any other form or medium, including, but not limited to, business processes, practices, methods, policies, plans, publications, documents, research, operations, services, strategies, techniques, agreements, contracts, transactions, potential transactions, know-how, trade secrets, databases, manuals, records, supplier information, financial information, accounting information, legal information, marketing information, pricing information, payroll information, personnel information, and supplier lists.

        14.  NON-SOLICITATION. Buyer agrees not to solicit or hire any personnel of MRP involved with the delivery of the Services during the provision of such Services and for twelve (12) months after the completion of such Services; provided, however, that Buyer may hire individuals employed by MRP who, without other solicitation, respond to advertisements or solicitations aimed at the general public.

        15.  EQUITABLE REMEDIES. Buyer acknowledges and agrees that (a) a breach or threatened breach by Buyer of any of its obligations under Sections 13 or 14 would give rise to irreparable harm to MRP for which monetary damages would not be an adequate remedy and (b) in the event of a breach or a threatened breach by Buyer of any such obligations, MRP shall, in addition to any and all other rights and remedies that may be available to MRP at law, at equity, or otherwise in respect of such breach, be entitled to equitable relief, including a temporary restraining order, an injunction, specific performance, and any other relief that may be available from a court of competent jurisdiction, without any requirement to post a bond or other security, and without any requirement to prove actual damages or that monetary damages will not afford an adequate remedy. Buyer agrees that Buyer will not oppose or otherwise challenge the appropriateness of equitable relief or the entry by a court of competent jurisdiction of an order granting equitable relief, in either case, consistent with the terms of this Section 15.

        16.  INDEMNIFICATION. Buyer agrees to indemnify, defend and hold harmless MRP and its directors, shareholders, employees and agents (collectively, “MRP Indemnitees”) against any liability, damage, loss or expense incurred by or imposed in connection with any claims, suits, actions, demands or judgments arising out of (a) any breach or non-fulfillment of any representation, warranty or covenant set forth in this Agreement by Buyer or its directors, managers, employees or agents (collectively, “Buyer’s Agents”); (b) any negligent act or omission or willful misconduct of Buyer or Buyer’s Agents in connection with this Agreement; (c) any bodily injury, death of any person or damage to real or tangible personal property caused by Buyer or Buyer’s Agents, including the use of unauthorized parts in or service of the Equipment; (d) any failure by Buyer or Buyer’s Agents to comply with any applicable laws; (e) any fraud or other intentional acts by Buyer or Buyer’s Agents; and (f) the use or operation of the Equipment, including, without limitation, any medical and/or surgical procedures performed by Buyer, and any of Buyer’s Agents, using the Equipment unless said damages are determined by a court of competence jurisdiction to be solely by the gross negligence of MRP or solely as result of a breach by MRP of the limited warranties contained herein.

        17.  DEFAULTS; REMEDIES. Notwithstanding anything herein to the contrary, should Buyer fail to pay for the order or any other amount, in whole or in part, when due or perform its other obligations under this Agreement or as otherwise mutually agreed in writing between Buyer and MRP (each, a “Default”), then MRP may take any and all actions available under law or equity to collect said amounts with a ten (10) day prior written notice, including, but not limited to, enforcing its security interest, accelerating the payment of and declaring immediately due and payable any unpaid balance of the order, referral to outside collection agencies and/or commencement of legal action. MRP’s rights shall be cumulative, and it shall not be required to have attempted to realize upon to the Equipment before taking any other collection actions. MRP may require that Buyer assemble and return any or all of the Equipment to MRP and, in the event Buyer fails to return such Equipment peaceably, enter upon the premises where such Equipment is located, with or without legal process, and repossess such Equipment. Upon a Default, Buyer agrees to pay upon MRP’s demand: (i) all costs and expenses incurred by MRP or its assignee in connection with the enforcement of any remedies, including all expenses incurred in connection with the return, sale, release or other disposition of the Equipment, including attorneys’ fees and other costs incurred by MRP or its assignee in enforcing or defending its rights and remedies under this Agreement and any other written agreement between Buyer and MRP.

        18.  COMPLIANCE WITH LAWS. Buyer shall (a) carry out the transactions contemplated by this sale and deal with the Equipment in conformity with all applicable laws, rules and regulations of all government authorities, including, without limitation, export laws, (b) obtain all permits and licenses required in connection with the purchase, shipment, installation or use of the Equipment, and (c) be solely responsible to fully understand and comply with laws, rules and regulations. Any information provided is as a convenience only.

        19.  FURTHER ASSURANCES. Upon MRP’s reasonable request, Buyer shall, at its sole cost and expense, execute and deliver all such further documents and instruments, and take all such further acts, necessary to give full effect to this Agreement.

        20.  ASSIGNMENT; SUCCESSORS AND ASSIGNS. Buyer cannot delegate any duties nor assign any rights or claims under this Agreement without MRP’s prior written consent, and any such attempt or assignment shall be void. In the event that Buyer finances its acquisition of any Equipment with a third party, Buyer may direct MRP to transfer title of such Equipment to such third-party financing company, with all remaining terms and conditions of this Agreement remaining in full force and effect. This Agreement is binding on and inures to the benefit of the parties to this Agreement and their respective permitted successors and permitted assigns.

        21.  NO THIRD-PARTY BENEFICIARIES. Subject to Section 16, this Agreement benefits solely the parties to this Agreement and their respective permitted successors and assigns, and nothing in this Agreement, express or implied, confers on any other person any legal or equitable right, benefit, or remedy of any nature whatsoever under or by reason of this Agreement.

        22.  GOVERNING LAW; VENUE. The application of the UN Convention on Contracts for the International Sale of Goods is expressly excluded. The parties agree that any and all claims, demands, disagreements, controversies or disputes arising out of or relating to this Agreement and any agreement or document delivered in connection herewith (collectively, “Claims”) shall be governed by and construed in accordance with the laws of the State of Utah and adjudicated exclusively in the state and federal courts located in or nearest to Summit County, Utah, which courts shall have the sole and exclusive jurisdiction and venue for adjudication of all Claims. The parties hereby agree upon, consent and stipulate to the jurisdiction and venue of the aforementioned courts for the adjudication of all Claims, to the exclusion of all other courts, forums and venues whatsoever.

        23.  NON-DISPARAGEMENT. Buyer shall not disparage MRP or MRP’s trademarks, websites, products or services, or display any such items in a derogatory or negative manner on any website or in any public forum or press release.

        24.  NOTICES. Any notice, demand, or communication required, permitted or desired to be given hereunder shall be deemed effectively given when personally delivered, when sent by electronic means, when received by overnight courier, or when mailed by prepaid, certified or registered mail, return receipt requested, addressed to the other party at its address set forth on the Quote or to such other address that the receiving party may designate from time to time in accordance with this Section 25.

        25.  PUBLIC ANNOUNCEMENTS. Unless otherwise stated herein, neither party shall issue a press release or otherwise advertise, make a public statement or disclose to any third-party information pertaining to the relationship arising under this Agreement, the existence or terms of this Agreement, the underlying transactions between MRP and Buyer or agent for Buyer or refer to the other party in relation to this Agreement without the other party’s prior written approval.

        26.  ENTIRE AGREEMENT; ADDITIONAL OR INCONSISTENT TERMS. Subject to Section 32, this Agreement constitutes the sole and entire agreement between the parties hereto relating to the subject matter hereof, and any unincorporated representation, affirmation of fact, course of prior dealings, promise or condition in connection therewith, or usage of the trade, shall not be binding on either party. Terms and conditions set forth which differ from, conflict with or are not included in this Agreement shall not be part of any agreement between MRP and Buyer unless both parties specifically accept such terms and conditions in writing.

        27.  WAIVER. No waiver under this Agreement is effective unless it is in writing and signed by the party waiving its right. Any waiver authorized on one occasion is effective only in that instance and only for the purpose stated and does not operate as a waiver on any future occasion. None of the following constitutes a waiver or estoppel of any right, remedy, power, privilege or condition arising from this Agreement: any failure or delay in exercising any right, remedy, power or privilege or in enforcing any condition under this Agreement; or any act, omission or course of dealing between the parties.

        28.  SURVIVAL. Subject to the limitations and other provisions of this Agreement, the representations and warranties of Buyer contained herein shall survive the expiration or earlier termination of this Agreement for a period of twelve (12) months after such expiration o termination and (b) this Section 29 and Sections 10, 12, 13, 14, 15, 16, 17, 21, 22, 23, 24, 26, and 32 of this Agreement, as well as any other provision that, in order to give proper effect to its intent, should survive such expiration or termination, shall survive the expiration or earlier termination of this Agreement. All other provisions of this Agreement shall not survive the expiration or earlier termination of this Agreement.

        29.  RELATIONSHIP OF PARTIES. Nothing in this Agreement creates any agency, joint venture, partnership or other form of joint enterprise, employment or fiduciary relationship between the parties. Neither party has any express or implied right or authority to assume or create any obligations on behalf of or in the name of the other party or to bind the other party to any contract, agreement or undertaking with any third party.

        30.  HEADINGS. The headings in this Agreement are for reference only and do not affect the interpretation of this Agreement.

        31.  ORDER OF PRECEDENCE. In the event of conflict between the Quote, a written agreement by MRP, and these Terms, the order of priority shall be: (1) the written

agreement by MRP, if only if executed by an MRP Officer, (2) the Quote and (3) these Terms, and only to the extent of the direct conflict. Notwithstanding the foregoing, MRP shall not be bound by, and specifically objects to, any terms, conditions or other provisions, both written and oral, which are different from, in addition to or inconsistent with the provisions of this Agreement which are set forth in any purchase order, receipt, acceptance, confirmation, correspondence or otherwise of, or by, Buyer. Fulfillment of Buyer’s order shall not constitute acceptance of any of Buyer’s terms and conditions and does not serve to modify or amend the terms and conditions contained herein.

        32.  SEVERABILITY. If any part of this Agreement is held to be void, illegal or unenforceable, then it shall be deemed to be severed from this Agreement and the remaining provisions shall continue in full force and effect; provided, however, that if any fundamental term or provision of this Agreement is held to be void, illegal or unenforceable, the remainder of this Agreement shall be unenforceable. Upon a determination that any term or provision is void, illegal or unenforceable, the parties shall negotiate in good faith to modify this Agreement to effect the original intent of the parties as closely as possible in order that the transactions contemplated hereby be consummated as originally contemplated to the greatest extent possible.