Видео ютуба по тегу Global Unique Device Identification Database

How to Submit Data to the Global Unique Device Identification Database

Unique Device Identification (UDI) - 21 CFR 1271.290

FDA Unique Device Identifier (UDI) Requirements

Implementing a Global Unique Device Identification (UDI) Solution: Regional Update and Requirements

Webinar: Introduction to FDA Unique Device Identification (UDI) Requirements Part II

TGA Webinar: Unique Device Identification UDI Webinar 2 - Considerations for the Australian UDI

Unique Device Identification Webinar #7 - Global manufacturer UDI learnings, 22 March 2022

Everything You Must Know About UDI & GUDID Compliance

Know Your Medical Device Why the Unique Device Identification UDI System Should Matter to You

EPISODE 5: Unique Device Identification Compliance Dates

FDA Webinar The Unique Device Identification Program UDI 101

Unique Device Identification #8 - Global manufacturer learnings and project update, 19 April 2022

TGA Webinar: Unique Device Identification #1

Unique Device Identification: How to Complete UDI Compliance by September 2016

Unique Device Identification UDI Requirements and Timelines

Unique Device Identification (UDI)

FDA Devices - Unique Device Identifier (UDI) for Patient Safety and Transformation

AccessGUDID: Search and Download

Understanding global UDI rules

Unique Device Identification #10 - Accessing and using the Australian UDI database, 21 June 2022

Unique Device Identification (UDI)

Unique Device Identification (UDI)

Exploring Medical Device UDI (Unique Device Identification)

FDA Webinar GUDID Device Identifier.#fda #cdrh #GUDID #DeviceIdentifier #medicaldevices #patient

Why is a UDI (Unique Device Identification) so Important?