Identity
- Trade Name
- Liquichek FDA UDI
- Generic Name
- Reticulocyte count IVD, control FDA UDI
- Device Name
- Liquichek Reticulocyte Control (A-I) Bilevel MiniPak (An assayed reticulocyte control.) FDA UDI
- Model / Reference
- 915X FDA UDI
- Description
- Liquichek Reticulocyte Control (A-I) Bilevel MiniPak (An assayed reticulocyte control.) FDA UDI
Identifiers
- Catalog Number
- 915X FDA UDI
- Primary DI / UDI-DI
- 00847661003793 FDA UDI
- 510(k) Number
- K010470 FDA UDI
- FDA Product Code
- JPK FDA UDI
- GMDN Term
- Reticulocyte count IVD, control FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.8625 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: Reticulocyte count IVD, control
Liquichek by Bio-Rad Laboratories — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K010470 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bio-Rad Laboratories
Sources (1)
- FDA UDI bc2088ed-171e-458f-8b16-63276941d816 37 fields · synced May 30, 2026