Providence Medical

global contract manufacturing

Clean Rooms

Providence Medical Clean Room FacilitiesProvidence Medical’s Multiple Class 100,000 (ISO Class 8) Clean Rooms are available for developing a variety of healthcare products, especially single-time use disposable devices. Facilities are fully maintained and certified as required by ISO 13485, 14644 and 14698. All Clean Room certification and maintenance records are available for your review.

In addition to medical device manufacturing, Providence Medical’s Clean Rooms may be used for related specialized needs, such as:

  • Sterile packaging
  • Pouch or blister/tray package and sealing production
  • Packaging validation
  • Sterilization validation, using outside sourcing of either Ethylene Oxide, Gamma or e-beam sterilization

Modular Environments

Our modular environments can accommodate a variety of manufacturing and production requirements — from light pilot production to substantial commercialized product builds — all finished in compliance with Good Manufacturing Practices (GMP), proper line clearance, lot history traceability and sterilization protocols. Unique to our sterilized disposable device development and manufacturing is the ability to incorporate sterilized disposables into a complete integrated system.

Contact us to learn more about our facilities.


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