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UDI Rule Announced

September 30, 2013 by QTS Medical Device Outsourcing

Unique Device Identification (UDI) Final Rule was announced by the FDA on September 20, 2013. The rule was published in the Code of Federal Regulations as of September 24, 2013. Implementation for Class III device labeling is required in 2014. Implementation for other device Classes follow per a defined schedule.

Read the full press release from the FDA.

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  • Services
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    • Materials Sourcing
    • Engineering Validations
    • Label Development & Printing
    • Critical Inspection Services
    • Cleaning & Passivation
    • Cleanroom Assembly, Kitting & Packaging
    • Sterilization Services
    • Lab Testing Services
    • Supply Chain Management
  • Our Approach
  • Quality
    • Procedural Guidelines
  • Resources
  • Careers
  • About
    • Vision and Values
    • Leadership
    • Power of Cretex Medical
  • Contact
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