Alinity 09P901A
by Abbott
Alinity 09P901A is a Class I device made by Abbott, listed in FDA GUDID since 10 Dec 2018 (UDI-DI 00380740152109), 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 | Number00380740152109 | Date10 Dec 2018 | StatusListed |
Official records
- AccessGUDID record 00380740152109
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Alinity
- Generic name
- Laboratory instrument/analyser application software IVD
- Model / Ref / Catalog
- 09P901A
- Primary DI / UDI-DI
- 00380740152109
- FDA product code
- JJE
- GMDN term
- Laboratory instrument/analyser application software IVD
- Device class
- Class I
- Regulation number
- 862.2160
- GUDID distribution status
- In Commercial Distribution
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