PremierPro 3702BM
PremierPro 3702BM is a Class I device made by Prestige Ameritech, listed in FDA GUDID since 22 Aug 2023 (UDI-DI 00811220034931), registry data as of 22 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 | Number00811220034931 | Date22 Aug 2023 | StatusListed |
Official records
- AccessGUDID record 00811220034931
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PremierPro
- Generic name
- Patient transfer system, manual
- Model / Ref / Catalog
- 3702BM
- Primary DI / UDI-DI
- 00811220034931
- FDA product code
- FMR
- GMDN term
- Patient transfer system, manual
- Device class
- Class I
- Regulation number
- 880.6785
- GUDID distribution status
- In Commercial Distribution
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