Immco Diagnostics 2308
Immco Diagnostics 2308 is a Class II device made by Immco Diagnostics, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00845714004353), 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 | Number00845714004353 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00845714004353
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Immco Diagnostics
- Generic name
- Buffered sample diluent IVD, manual
- Model / Ref / Catalog
- 2308
- Primary DI / UDI-DI
- 00845714004353
- FDA product code
- MSV, LJM
- GMDN term
- Buffered sample diluent IVD, manual
- Device class
- Class II
- Regulation number
- 866.5660, 866.5100
- GUDID distribution status
- In Commercial Distribution
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