Fresh Cells 51-2418
Fresh Cells 51-2418 is a Class I device made by Diagnostic Hybrids, Inc., listed in FDA GUDID since 21 Sep 2018 (UDI-DI 30014613332305), 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 | Number30014613332305 | Date21 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 30014613332305
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Fresh Cells
- Generic name
- Cell culture line IVD
- Model / Ref / Catalog
- 51-2418
- Primary DI / UDI-DI
- 30014613332305
- FDA product code
- KIR
- GMDN term
- Cell culture line IVD
- Device class
- Class I
- Regulation number
- 864.2280
- GUDID distribution status
- In Commercial Distribution
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