Unyvero M1 Master Mix Tube Kit
by Curetis GmbH GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04260364750041 | Date28 May 2018 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 23 Oct 2026.
Specification
- Trade Name
- Unyvero
- Generic Name
- DNA amplification enzyme reagent IVD
- Model / Ref / Catalog
- M1 Master Mix Tube Kit, 10020
- Primary DI / UDI-DI
- 04260364750041
- FDA Product Code
- QBH
- GMDN Term
- DNA amplification enzyme reagent IVD
- Device Class
- Class II
- Regulation Number
- 866.3985
- Commercial Distribution
- Not in Commercial Distribution
Other devices from Curetis GmbH
Properties
Other properties (9)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No