Identity
- Trade Name
- Liquichek FDA UDI
- Generic Name
- Multiple immunosuppressant therapeutic drug monitoring IVD, control FDA UDI
- Device Name
- Liquichek Whole Blood Immunosuppressant Control Level 3 (A human whole blood assayed control.) FDA UDI
- Model / Reference
- 12000406 FDA UDI
- Description
- Liquichek Whole Blood Immunosuppressant Control Level 3 (A human whole blood assayed control.) FDA UDI
Identifiers
- Catalog Number
- 12000406 FDA UDI
- Primary DI / UDI-DI
- 00847661005803 FDA UDI
- 510(k) Number
- K121143 FDA UDI
- FDA Product Code
- DIF FDA UDI
- GMDN Term
- Multiple immunosuppressant therapeutic drug monitoring IVD, control FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.3280 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
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
Category: Multiple immunosuppressant therapeutic drug monitoring IVD, control
Liquichek by Bio-Rad Laboratories — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K121143 also covers:
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bio-Rad Laboratories
Sources (1)
- FDA UDI 9dc0d84f-c3d4-4118-8eea-e645ae557fc2 37 fields · synced May 30, 2026