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Freelite® Human Lambda Free Kit for use on the Roche cobas® c systems – Bulk Kit
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Freelite® Human Lambda Free Kit for use on the Roche cobas® c systems – Bulk Kit FDA UDI
- Generic Name
- Kappa/lambda light chain immunoglobulin IVD, kit, nephelometry/turbidimetry FDA UDI
- Model / Reference
- LK018.10CB FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05051700016070 FDA UDI
- 510(k) Number
- K040009 FDA UDI
- FDA Product Code
- DEH FDA UDI
- GMDN Term
- Kappa/lambda light chain immunoglobulin IVD, kit, nephelometry/turbidimetry FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.5550 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Freelite® Human Lambda Free Kit for use on the Roche cobas® c systems – Bulk Kit by The Binding Site Group — Class II — FDA UDI — listed in FDA GUDID
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- The Binding Site Group
Sources (1)
- FDA UDI 7bee2473-5fa2-4114-a89e-812b8f8e7430 36 fields · synced May 30, 2026