← Back to catalogue
Light Diagnostics™ Simulfluor® HSV 1/ HSV 2 DFA Kit
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Light Diagnostics™ Simulfluor® HSV 1/ HSV 2 DFA Kit FDA UDI
- Generic Name
- Herpes simplex virus 1 & 2 (HSV1 & 2) antigen IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- Simulfluor HSV 1/ HSV 2 DFA Kit FDA UDI
- Model / Reference
- 3293 FDA UDI
- Description
- Simulfluor HSV 1/ HSV 2 DFA Kit FDA UDI
Identifiers
- Catalog Number
- 3293 FDA UDI
- Primary DI / UDI-DI
- 04053252589942 FDA UDI
- 510(k) Number
- K991880 FDA UDI
- FDA Product Code
- GQN 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
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
Light Diagnostics™ Simulfluor® HSV 1/ HSV 2 DFA Kit by Emd Millipore Corporation — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Emd Millipore Corporation
Sources (1)
- FDA UDI d4fbc65f-bdf6-41af-83dc-6cc50cef2b2a 37 fields · synced May 31, 2026