PremierPro 8974
PremierPro 8974 is a Class I device made by Prestige Ameritech, listed in FDA GUDID since 29 Aug 2020 (UDI-DI 00818566016805), 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 | Number00818566016805 | Date29 Aug 2020 | StatusListed |
Official records
- AccessGUDID record 00818566016805
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PremierPro
- Generic name
- Non-adhesive device retention bandage
- Model / Ref / Catalog
- 8974
- Primary DI / UDI-DI
- 00818566016805
- FDA product code
- FQM, KGX
- GMDN term
- Non-adhesive device retention bandage
- Device class
- Class I
- Regulation number
- 880.5075, 880.5240
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code FQM (Bandage, Elastic).
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- SOF-BAND HIGH STRETCH BANDAGES by Johnson & Johnson Professionals, Inc.
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- ANAGO DISP., ALL PURPOSE PATIENT REST. by Anago, Inc.
- SECUTEX SURGICAL BINDER by Conphar, Inc.
- BANDAGE, RAPIDO-LASTIC COTTON/NYLON by Conco Medical Co.
- BANDAGE, CONFO-LASTIC ALL COTTON ELASTIC by Conco Medical Co.
- TUBULAR BANDAGE by Secol Co.
- ORTHO WRAP by Fast Wrap Co., Inc.
- BINDAFIX by Conphar, Inc.