PremierPro™ 31C18125
PremierPro™ 31C18125 is a Class II device made by Prestige Ameritech, listed in FDA GUDID since 7 Jul 2022 (UDI-DI 00811220033798), 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 | Number00811220033798 | Date7 Jul 2022 | StatusListed |
Official records
- AccessGUDID record 00811220033798
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PremierPro™
- Generic name
- Intravenous line recessed-needle connector
- Model / Ref / Catalog
- 31C18125
- Primary DI / UDI-DI
- 00811220033798
- FDA product code
- FOZ
- GMDN term
- Intravenous line recessed-needle connector
- Device class
- Class II
- Regulation number
- 880.5200
- GUDID distribution status
- In Commercial Distribution
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