Remanufacturing of Medical Devices: Guidance for Industry, Entities That Perform Servicing or Remanufacturing, and Food and Drug Administration Staff
Information
Type
Guidance
Regulated products
Medical Devices
Topics
Labeling
Published
May 10, 2024
Last updated
May 9, 2024
Description
A guidance document focusing on labeling requirements for the remanufacturing of medical devices, aimed at industry entities and FDA staff.
Tags
Organization
Country / Region
United States
License
Other (Public Domain)