Identity
- Trade Name
- Liquichek FDA UDI
- Generic Name
- C-reactive protein (CRP) IVD, control FDA UDI
- Device Name
- Liquichek Elevated CRP Control Level 1 (A human serum C-Reactive Protein control.) FDA UDI
- Model / Reference
- 254 FDA UDI
- Description
- Liquichek Elevated CRP Control Level 1 (A human serum C-Reactive Protein control.) FDA UDI
Identifiers
- Catalog Number
- 254 FDA UDI
- Primary DI / UDI-DI
- 00847661000914 FDA UDI
- 510(k) Number
- K042837 FDA UDI
- FDA Product Code
- JJX FDA UDI
- GMDN Term
- C-reactive protein (CRP) IVD, control FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1660 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: C-reactive protein (CRP) IVD, control
Liquichek by Bio-Rad Laboratories — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as C-reactive protein (CRP) IVD, control.
- ASI CRP Control Set — Arlington Scientific, Inc. · Class II
- K-ASSAY® hsCRP Control — KAMIYA BIOMEDICAL COMPANY, LLC · Class I
- HIGH SENSITIVITY CRP CONTROL - LEVEL II (hsCRP CONTROL 2) — Randox Laboratories, Ltd. · Class I
- Audit MicroControls Linearity LQ hs-CRP — Aalto Scientific, Ltd.
- Diazyme — Diazyme Laboratories, Inc.
- POINTE SCIENTIFIC CRP Control Set — POINTE SCIENTIFIC, INC. · Class II
- IMMULITE® Systems CRP CONTROL C-Reactive Protein — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class II
- DImension Vista® High Sensitivity CRP Control H (high) — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class I
Cleared under the same submission
K042837 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 |
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Manufacturer
- Manufacturer
- Bio-Rad Laboratories
Sources (1)
- FDA UDI 92e6133e-4255-49d4-b184-bc76d07d0e59 37 fields · synced Jun 1, 2026