Intended for healthcare professionals

Sustainability Solutions

Built on a foundation of trusted original equipment manufacturer (OEM) expertise, Johnson & Johnson MedTech is elevating electrophysiology (EP) reprocessing (RPO) with a commitment to your success, by delivering an RPO experience that is indiscernible from the OEM.1-3


Our dedicated, highly-skilled RPO team partners closely with supply chain leaders to provide precision products, powerful savings and tangible sustainability benefits, helping your organization optimize resources while reducing environmental impact.

Sustainability Solutions
Sustainability Solutions

Electrophysiology requires a specialized reprocessor

EP procedures are technically and clinically complex, demanding the highest standards—there’s no room for compromise. Choosing the wrong partner may lead to uncertainty in clinician trust and program savings.


With Johnson & Johnson MedTech's Sustainability Solutions, you’re not just reprocessing devices — you're elevating your entire EP program with a trusted partner. We are dedicated to the highest reliability and safety standards, giving clinicians the confidence they need to deliver exceptional patient care.

Feel secure

Partnering with the leading^ OEM and RPO Manufacturer for EP Devices.

≤1mm

Location accuracy for Certified Performance Reprocessed mapping catheters as compared to the OEM catheter.1-3

100%

Assurance that Certified Performance Devices are functionally tested using OEM proprietary testing equipment and specifications.1-3

100%

Of RPO EP spend counts towards J&J MedTech EP OEM contract performance.4

100%

Program support provided for optimal RPO program effectiveness and technically and clinically demanding EP OEM and RPO clinical cases.5

OEM standards in EP reprocessing

Together, we can maximize the value of your EP reprocessing program

Product precision: Precision isn’t just a feature - it’s our foundation. Our proprietary Certified Performance Program guarantees that EP reprocessed catheters are calibrated and tested to OEM specifications, ensuring consistent, reliable performance that maintains physician trust.

Powerful savings: J&J MedTech empowers customers to combine purchases across OEM and RPO EP contracts, unlocking considerable savings. This approach ensures EP reprocessing contracts complement OEM contracts, preserving volume commitments. 

Partner excellence: Clinical Account Specialists and dedicated RPO field service team members partner with you to optimize collections, improving your program effectiveness and advancing a circular economy.

Sustainability Solutions
I value partnering with suppliers that have shared goals.  J&J MedTech and my EP lab openly collaborate to advance patient care, control costs, and support the environment.

Yolanda D.,  Supply Chain Clinical Transformation, Cardiovascular

Reliability in every step

Seamless collection & inspection
Step 1

Seamless collection & inspection

Our strategically placed bins make the process effortless. Collections are managed by our highly trained CAS team, every step is handled with precision—so your staff can focus on what they do best. Full bins are securely transported to our state-of-the-art reprocessing facilities. There, our expert technicians inspect each device, ensuring only the highest quality items move forward.

Precision cleaning & decontamination
Step 2

Precision cleaning & decontamination

Once devices pass our initial inspection, they move to the critical cleaning and decontamination stage. Here, they undergo a series of rigorously validated steps designed to ensure the highest standards of quality and safety. Every step in the process is carefully monitored to guarantee your J&J MedTech EP Certified Performance devices are consistent with OEM standards.

OEM standard functional testing
Step 3

OEM standard functional testing

Every device we reprocess undergoes comprehensive functional testing to ensure quality and performance. Certified Performance devices are tested to OEM standards, utilizing proprietary OEM testing equipment to guarantee precision and reliability.

Packaging, sterilization & quality assurance
Step 4

Packaging, sterilization & quality assurance

After passing functional verification, devices are carefully packaged, ensuring integrity and protection. They are then sent for sterilization, and once sterilization is verified, each device undergoes a final multi-point inspection. Only after passing this quality check are the devices delivered to your EP lab—ready for use.

Frequently asked questions

Contact our team

We are on a mission to unite like-minded organizations committed to driving sustainable innovation by advancing a circular economy.

Customer Service

1-888-541-0078

Collections Support

References

^ Based on 2024 Clarivate market share data

* Using a reprocessed single use electrophysiology medical device can save up to 50% on carbon emissions when compared to an Original Equipment Manufactured device.

** Estimated savings are modelled using data from customers who exhibit high levels of program performance.

i. Based on a comparative study done in Portugal in 2014 (N=733) Based on a comparative study done in Portugal in 2014 (N=733)

  1. J&J MedTech R&D Certified Performance Overview - Decanav. Windchill #502385153
  2. J&J MedTech R&D Certified Performance Overview - Pentaray. Windchill #502385140
  3. J&J MedTech R&D Certified Performance Overview - Soundstar and Lasso. Windchill #502472542
  4. J&J MedTech Contracting Memo
  5. CAS Collection Memo - Sustainability
  6. Reprocessing of Single Use Medical Devices - Clinical and Financial
  7. Kicak, Katherine. Screening LCA of Single-Use Medical Devices Disposed Versus Being Reprocessed.2024; Slide 24. 06/10/2025.

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