← Back to catalogue

ASI VZV IgG EIA Test

FDA UDI

Class II (US FDA UDI)

by Arlington Scientific, Inc.

Identity

Trade Name
ASI VZV IgG EIA Test FDA UDI
Generic Name
Varicella-zoster virus (VZV) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Detection of Varicella Zoster Antibody FDA UDI
Model / Reference
NC-840096-AG FDA UDI
Description
Detection of Varicella Zoster Antibody FDA UDI

Identifiers

Catalog Number
NC-840096-AG FDA UDI
Primary DI / UDI-DI
00816057020584 FDA UDI
510(k) Number
K972295 FDA UDI
FDA Product Code
LFY FDA UDI
GMDN Term
Varicella-zoster virus (VZV) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3900 FDA UDI
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

No

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 G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

ASI VZV IgG EIA Test by Arlington Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Varicella-zoster virus (VZV) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA).

Cleared under the same submission

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 974d84f8-938c-40df-a5ee-450a1e291684 38 fields · synced Jul 18, 2026