CDSCO G.S.R.G.S.R. 918(E)
G.S.R. 918(E) is the official CDSCO identifier for “Medical Devices (Amendment) Rules, 2021”. G.S.R. 918(E) is the official identifier CDSCO uses for this instrument.
- Instrument
- G.S.R.
- Full name
- G.S.R. 918(E)
- Category
- UDI
- Authority source
- English
- Readable HTML
- 0 articles · 1 language version
- Published
- 31 December 2021
- Effective
- 1 January 2022
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Each version has stable article anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.
Medical Devices (Amendment) Rules, 2021
G.S.R. 918(E) of 31 December 2021 amends rule 46 to require unique device identification of medical devices, with UDI-DI to be declared on labels in a phased manner. Official gazette PDF ingested as corpus text.
G.S.R. 918(E) is the official identifier CDSCO uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.