Customed 712057342981
Customed 712057342981 (9002981) is a Class II device made by Customed, Inc., listed in FDA GUDID since 23 Sep 2016 (UDI-DI M20890029812), 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 | NumberM20890029812 | Date23 Sep 2016 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Customed
- Generic name
- Basic electric home bed
- Model / Ref / Catalog
- 712057342981, 9002981
- Primary DI / UDI-DI
- M20890029812
- FDA product code
- FNL
- GMDN term
- Basic electric home bed
- Device class
- Class II
- Regulation number
- 880.5100
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code FNL (Bed, Ac-Powered Adjustable Hospital).
- VOLKER NURSING BED MODEL 2080E & 2090E by Volker Healthcare, Inc.
- SOMA SAFE ENCLOSURE by Nova Technology Corp.
- iBed Wireless with iBed Mobile by Stryker Corp.
- MEGABED 1000 by Surgimed, Inc.
- Aolike ALK-BA501EZT by Zhongshan Aolike Medical Equipment Technology Co., Ltd
- PNEUMATIC/ELECTRIC/HYDRAULIC BED by G.W. Healthcare, Inc.
- TOTALCARE by HILL-ROM, INC.
- STRYKER AGILITY INTENSIVE CARE BED by Stryker Medical
- IBED WIRELESS WITH IBED AWARENESS by Stryker Corp.
- CARROM CARELIFE SERIES 40000 MODULAR BES SYSTEM by Carrom Healthcare, Inc.