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Anti-Insulin ELISA

FDA UDI

Class I (US FDA UDI)

by DRG International, Inc.

Identity

Trade Name
Anti-Insulin ELISA FDA UDI
Generic Name
Insulin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Anti-Insulin ELISA is a test system for the quantitative measurement of IgG class autoantibodies against insulin in human serum or plasma. FDA UDI
Model / Reference
EIA-3608 FDA UDI
Description
Anti-Insulin ELISA is a test system for the quantitative measurement of IgG class autoantibodies against insulin in human serum or plasma. FDA UDI

Identifiers

Catalog Number
EIA-3608 FDA UDI
Primary DI / UDI-DI
00840239036087 FDA UDI
FDA Product Code
CFP FDA UDI
GMDN Term
Insulin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1405 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

Yes

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

Yes

FDA UDI

Category: Insulin antibody IVD, kit, enzyme immunoassay (EIA)

Anti-Insulin ELISA by DRG International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Insulin antibody IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI db8da030-bcfd-462c-bac2-15c553d904ac 36 fields · synced May 30, 2026