Identity
- Trade Name
- Bartels® FDA UDI
- Generic Name
- Herpes simplex virus 1 & 2 (HSV1 & 2) antigen IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- Bartels® HSV Fluorescent Monoclonal Antibody Test FDA UDI
- Model / Reference
- B1029-48 FDA UDI
- Description
- Bartels® HSV Fluorescent Monoclonal Antibody Test FDA UDI
Identifiers
- Catalog Number
- B1029-48 FDA UDI
- Primary DI / UDI-DI
- 05391516745932 FDA UDI
- FDA Product Code
- GQL FDA UDI
- GMDN Term
- Herpes simplex virus 1 & 2 (HSV1 & 2) antigen IVD, kit, fluorescent immunoassay FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3305 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Bartels® by Trinity Biotech Public Limited Company — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Trinity Biotech Public Limited Company
Sources (1)
- FDA UDI 222c663f-b9b6-48b9-9c6f-1b1e8cbdcfb9 38 fields · synced Jun 1, 2026