EDA EDREX:EDREX: GL.CAMD.005
EDREX: GL.CAMD.005 is the official EDA identifier for “Regulatory Guideline on Requirements for Unique Device Identification (UDI) for Medical Devices”. EDREX: GL.CAMD.005 is the official identifier EDA uses for this instrument.
- Instrument
- EDREX:
- Full name
- EDREX: GL.CAMD.005
- Category
- UDI
- Authority source
- English
- Readable HTML
- 0 articles · 1 language version
- Published
- May 2026
- Effective
- May 2026
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Regulatory Guideline on Requirements for Unique Device Identification (UDI) for Medical Devices
EDREX: GL.CAMD.005 version 02/2026 (issued 05/2026; 21 pages), issued under EDA chairman decree 499 of 2021: UDI requirements for all medical devices, accessories, and IVDs supplied to the Egyptian market — Chapter One (UDI-DI and production identifier, issuing entities, data carriers and direct part marking), Chapter Two (additional labeling requirements), Chapter Three (import and distribution control), Chapter Four (compliance dates), Chapter Five (UDI in healthcare delivery), and the definitions/abbreviations annex. Applies to manufacturers, agents, importers, distributors, and healthcare providers. URL updated to the current v02/2026 file on the official guidelines index; the previously recorded media URL is a stale hash that now returns the Arabic homepage.
EDREX: GL.CAMD.005 is the official identifier EDA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.