← Back to catalogue

D3

FDA UDI

Class I (US FDA UDI)

by Diagnostic Hybrids, Inc.

Identity

Trade Name
D3 FDA UDI
Generic Name
Varicella-zoster virus (VZV) antigen IVD, control FDA UDI
Device Name
VZV Control Stock (Single Use) (shipped frozen) FDA UDI
Model / Reference
20-4600010 FDA UDI
Description
VZV Control Stock (Single Use) (shipped frozen) FDA UDI

Identifiers

Catalog Number
20-4600010 FDA UDI
Primary DI / UDI-DI
30014613338499 FDA UDI
FDA Product Code
OHQ FDA UDI
GMDN Term
Varicella-zoster virus (VZV) antigen IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

Yes

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) antigen IVD, control

D3 by Diagnostic Hybrids, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Varicella-zoster virus (VZV) antigen IVD, control.

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 b8a69e45-bd86-4d71-864c-44b5843bede5 35 fields · synced Jun 1, 2026