Acuitas
by Curetis GmbH GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04260364751017 | Date17 Apr 2023 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 21 Oct 2026.
Specification
- Generic Name
- Thermal cycler nucleic acid amplification analyser IVD, laboratory
- Model / Ref / Catalog
- Curetis Qualified QuantStudio™ 5 Real-Time PCR System, 62006
- Primary DI / UDI-DI
- 04260364751017
- 510(k) Number
- FDA Product Code
- OOI
- GMDN Term
- Thermal cycler nucleic acid amplification analyser IVD, laboratory
- Device Class
- Class II
- Regulation Number
- 862.2570
- Commercial Distribution
- Not in Commercial Distribution
Other devices from Curetis GmbH
Properties
Other properties (12)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No
- Manufacturing Date: No