Vitros 6808889
Vitros 6808889 is a Class II device made by Ortho-Clinical Diagnostics, listed in FDA GUDID since 28 Mar 2023 (UDI-DI 10758750033799), 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 | Number10758750033799 | Date28 Mar 2023 | StatusListed |
Official records
- AccessGUDID record 10758750033799
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Vitros
- Generic name
- Total triiodothyronine (TT3) IVD, kit, chemiluminescent immunoassay
- Model / Ref / Catalog
- 6808889
- Primary DI / UDI-DI
- 10758750033799
- FDA product code
- JIS
- GMDN term
- Total triiodothyronine (TT3) IVD, kit, chemiluminescent immunoassay
- Device class
- Class II
- Regulation number
- 862.1150
- GUDID distribution status
- In Commercial Distribution
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