Bam REV00
Bam REV00 (Z0156K1) is a Class I device made by Ehob, Inc., listed in FDA GUDID since 3 Sep 2024 (UDI-DI 10603354130521), 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 | Number10603354130521 | Date3 Sep 2024 | StatusListed |
Official records
- AccessGUDID record 10603354130521
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Bam
- Generic name
- Patient transfer system, manual
- Model / Ref / Catalog
- REV00, Z0156K1
- Primary DI / UDI-DI
- 10603354130521
- FDA product code
- FMR
- GMDN term
- Patient transfer system, manual
- Device class
- Class I
- Regulation number
- 880.6785
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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