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AccuDiag ™

FDA UDI

Class I (US FDA UDI)

by Diagnostic Automation, Inc.

Identity

Trade Name
AccuDiag ™ FDA UDI
Generic Name
Total testosterone IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
AccuDiag ™Testeosterone ELISA Kit FDA UDI
Model / Reference
DACD2095-18 FDA UDI
Description
AccuDiag ™Testeosterone ELISA Kit FDA UDI

Identifiers

Catalog Number
2095-18 FDA UDI
Primary DI / UDI-DI
00894175000817 FDA UDI
FDA Product Code
CDZ FDA UDI
GMDN Term
Total testosterone IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1680 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

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: Total testosterone IVD, kit, enzyme immunoassay (EIA)

AccuDiag ™ by Diagnostic Automation, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total testosterone IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diagnostic Automation, Inc.

Sources (1)

  • FDA UDI 91e87796-4c23-4587-8d9a-70f2b2094134 36 fields · synced May 30, 2026