← Back to catalogue

Light Diagnostics SimulFluor HSV/VZV Reagent

FDA UDI

Class II (US FDA UDI)

by Emd Millipore Corporation

Identity

Trade Name
Light Diagnostics SimulFluor HSV/VZV Reagent FDA UDI
Generic Name
Herpes simplex virus 1 & 2 (HSV1 & 2) antigen IVD, kit, fluorescent immunoassay FDA UDI
Device Name
SimulFluor HSV/VZV Reagent FDA UDI
Model / Reference
5235 FDA UDI
Description
SimulFluor HSV/VZV Reagent FDA UDI

Identifiers

Catalog Number
5235 FDA UDI
Primary DI / UDI-DI
04053252370960 FDA UDI
FDA Product Code
GQW 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
866.3900 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/VZV Reagent 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI ceaf2b11-fd34-4522-8cc9-583bd53b57d6 36 fields · synced May 30, 2026