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Insulin

FDA UDI

Class I (US FDA UDI)

by DRG International, Inc.

Identity

Trade Name
Insulin FDA UDI
Generic Name
Insulin IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
The DRG:HYBRId-XL Insulin is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of Insulin in serum and plasma (EDTA and Heparin). FDA UDI
Model / Reference
HYE-5361 FDA UDI
Description
The DRG:HYBRId-XL Insulin is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of Insulin in serum and plasma (EDTA and Heparin). FDA UDI

Identifiers

Catalog Number
HYE-5361 FDA UDI
Primary DI / UDI-DI
00840239053619 FDA UDI
FDA Product Code
CFP FDA UDI
GMDN Term
Insulin 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 IVD, kit, enzyme immunoassay (EIA)

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

Similar devices

Also classified as Insulin 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 bdaf6d89-11ee-491f-8bc1-a24921a12663 36 fields · synced May 30, 2026