Identity
- Trade Name
- LiquidQC NEPHROCHECK Control FDA UDI
- Generic Name
- Multiple acute kidney injury (AKI) marker IVD, control FDA UDI
- Device Name
- LiquidQC™ NEPHROCHECK® Control For VIDAS® 3 FDA UDI
- Model / Reference
- 83938 FDA UDI
- Description
- LiquidQC™ NEPHROCHECK® Control For VIDAS® 3 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817238010257 FDA UDI
- GMDN Term
- Multiple acute kidney injury (AKI) marker IVD, control FDA UDI
Classification
- Commercial Distribution
- 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
No
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
Yes
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 acute kidney injury (AKI) marker IVD, control
LiquidQC NEPHROCHECK Control by Cliniqa Corporation — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Multiple acute kidney injury (AKI) marker IVD, control.
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Cliniqa Corporation
Sources (1)
- FDA UDI b71e2efa-c24f-4fa1-b3be-55ad927c51ab 33 fields · synced Jun 8, 2026