Freelite® Human Lambda Free Kit for use on the Roche cobas® c Systems LK018.CB.A
Listed
Valid until
Not applicable
FDA recalls
None ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05051700021111 | Date2 Feb 2026 | StatusListed |
Recalls
-
- Terminated Z-2030-2021
The high and low level "Quality Controls" demonstrate a positive bias of approximately 10% compared to assigned values.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Freelite® Human Lambda Free Kit for use on the Roche cobas® c Systems
- Generic Name
- Kappa/lambda light chain immunoglobulin IVD, kit, nephelometry/turbidimetry
- Model / Reference
- LK018.CB.A
- Primary DI / UDI-DI
- 05051700021111
- 510(k) Number
- FDA Product Code
- DEH
- GMDN Term
- Kappa/lambda light chain immunoglobulin IVD, kit, nephelometry/turbidimetry
- Device Class
- Class II
- Regulation Number
- 866.5550
- GUDID distribution status
- In Commercial Distribution
Other devices from The Binding Site Group
Properties
Other properties (10)
- Sterile: No
- Single Use: 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