PremierPro 1241PP
PremierPro 1241PP is a Class II device made by Prestige Ameritech, listed in FDA GUDID since 4 Sep 2020 (UDI-DI 00811220030087), 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 | Number00811220030087 | Date4 Sep 2020 | StatusListed |
Official records
- AccessGUDID record 00811220030087
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PremierPro
- Generic name
- Circulating-fluid localized thermal therapy system control unit
- Model / Ref / Catalog
- 1241PP
- Primary DI / UDI-DI
- 00811220030087
- FDA product code
- ILO
- GMDN term
- Circulating-fluid localized thermal therapy system control unit
- Device class
- Class II
- Regulation number
- 890.5720
- GUDID distribution status
- In Commercial Distribution
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