PremierPro Lancet 7553
PremierPro Lancet 7553 is a Class II device made by Prestige Ameritech, listed in FDA GUDID since 3 Aug 2018 (UDI-DI 00811220030377), 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 | Number00811220030377 | Date3 Aug 2018 | StatusListed |
Official records
- AccessGUDID record 00811220030377
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PremierPro Lancet
- Generic name
- Blood lancing device tip
- Model / Ref / Catalog
- 7553
- Primary DI / UDI-DI
- 00811220030377
- FDA product code
- FMK
- GMDN term
- Blood lancing device tip
- Device class
- Class II
- Regulation number
- 878.4850
- GUDID distribution status
- In Commercial Distribution
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