Customed 712057104052
Customed 712057104052 (9004052) is a Class I device made by Customed, Inc., listed in FDA GUDID since 10 Aug 2023 (UDI-DI M20890040522), 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 | NumberM20890040522 | Date10 Aug 2023 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Customed
- Generic name
- Absorbent underpad, non-antimicrobial, single-use
- Model / Ref / Catalog
- 712057104052, 9004052
- Primary DI / UDI-DI
- M20890040522
- FDA product code
- KME
- GMDN term
- Absorbent underpad, non-antimicrobial, single-use
- Device class
- Class I
- Regulation number
- 880.6060
- GUDID distribution status
- In Commercial Distribution
Similar devices
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- AUTO TRAUMA KIT by Marshall Electronics, Inc.
- DISPOSE-A-SHEET by Belmac Healthcare Corp.
- ROSEALAE by Asmb
- DISPOSABLE UNDERPADS by Burina
- FOIL BABY BUNTING by Gam Industries, Inc.
- FLUFF UNDERPAD TYPE UP1001 by Bio D Corp.