Identity
- Trade Name
- VeriQuick FDA UDI
- Generic Name
- Varicella-zoster virus (VZV) immunoglobulin A (IgA) antibody IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- Ovulation Preedictor FDA UDI
- Model / Reference
- 11013002B FDA UDI
- Description
- Ovulation Preedictor FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00049696712682 FDA UDI
- FDA Product Code
- NGE FDA UDI
- GMDN Term
- Varicella-zoster virus (VZV) immunoglobulin A (IgA) antibody IVD, kit, fluorescent immunoassay FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1485 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
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: Varicella-zoster virus (VZV) immunoglobulin A (IgA) antibody IVD, kit, fluorescent immunoassay
VeriQuick by Fourstar Group Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Fourstar Group Inc.
Sources (1)
- FDA UDI 97d0b283-5506-46c4-829a-0d0df2074db1 33 fields · synced May 30, 2026