Immco Diagnostics 5305
Immco Diagnostics 5305 is a Class II device made by Immco Diagnostics, Inc., listed in FDA GUDID since 15 Nov 2016 (UDI-DI 00845714002953), 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 | Number00845714002953 | Date15 Nov 2016 | StatusListed |
Official records
- AccessGUDID record 00845714002953
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- Withdrawn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
- 5305
- Primary DI / UDI-DI
- 00845714002953
- FDA product code
- MID
- GMDN term
- Buffered sample diluent IVD, manual
- Device class
- Class II
- Regulation number
- 866.5660
- GUDID distribution status
- In Commercial Distribution
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