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D3

FDA UDI

Class I (US FDA UDI)

by Diagnostic Hybrids, Inc.

Identity

Trade Name
D3 FDA UDI
Generic Name
Adenovirus antigen IVD, control FDA UDI
Device Name
Adenovirus Control Stock FDA UDI
Model / Reference
20-4740010 FDA UDI
Description
Adenovirus Control Stock FDA UDI

Identifiers

Catalog Number
20-4740010 FDA UDI
Primary DI / UDI-DI
30014613338543 FDA UDI
FDA Product Code
OHQ FDA UDI
GMDN Term
Adenovirus 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: Adenovirus 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 Adenovirus antigen IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5278a558-c5a2-403d-afac-a56251a9b440 35 fields · synced May 31, 2026