Remanufacturing of Medical Devices: Guidance for Industry, Entities That Perform Servicing or Remanufacturing, and Food and Drug Administration Staff From Food and Drug Administration (FDA) πΊπΈ A guidance document focusing on labeling requirements for the remanufacturing of medical devices, aimed at industry entities and FDA staff. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 55.55555555555556/100 Updated on May 9, 2024 Other (Public Domain) 0 reuses 0 favorites
Points to Consider for the Preparation of Applications for Marketing Approval of Remanufactured Single-use Medical Devices From Pharmaceuticals and Medical Devices Agency (PMDA) π―π΅ PSEHB/MDE Notification No. 0816-3 Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 44.44444444444444/100 Updated on August 16, 2017 Other (Public Domain) 0 reuses 0 favorites