Customed 712057700051
Customed 712057700051 (9004051C) is a Class I device made by Customed, Inc., listed in FDA GUDID since 10 Aug 2023 (UDI-DI M2089004051C1), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberM2089004051C1 | Date10 Aug 2023 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Customed
- Generic name
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial
- Model / Ref / Catalog
- 712057700051, 9004051C
- Primary DI / UDI-DI
- M2089004051C1
- FDA product code
- LZA
- GMDN term
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial
- Device class
- Class I
- Regulation number
- 880.6250
- GUDID distribution status
- In Commercial Distribution
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