3CP™ Centrifuge 1
by Reapplix ApS
3CP™ Centrifuge 1 is a Class I device made by Reapplix ApS, listed in FDA GUDID since 19 Jul 2018 (UDI-DI 05714188021577), registry data as of 22 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 | Number05714188021577 | Date19 Jul 2018 | StatusListed |
Official records
- AccessGUDID record 05714188021577
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- 3CP™ Centrifuge
- Generic name
- Haematological concentrate system centrifuge
- Model / reference
- 1
- Primary DI / UDI-DI
- 05714188021577
- FDA product code
- JQC
- GMDN term
- Haematological concentrate system centrifuge
- Device class
- Class I
- Regulation number
- 862.2050
- GUDID distribution status
- In Commercial Distribution
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