← Back to catalogue

ACTH (Adrenocorticotropic Hormone) ELISA

FDA UDI

Class II (US FDA UDI)

by DRG International, Inc.

Identity

Trade Name
ACTH (Adrenocorticotropic Hormone) ELISA FDA UDI
Generic Name
Adrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
The DRG ACTH ELISA is intended for the quantitative determination of ACTH (Adreno-corticotropic Hormone) in human plasma. FDA UDI
Model / Reference
EIA-3647 FDA UDI
Description
The DRG ACTH ELISA is intended for the quantitative determination of ACTH (Adreno-corticotropic Hormone) in human plasma. FDA UDI

Identifiers

Catalog Number
EIA-3647 FDA UDI
Primary DI / UDI-DI
00840239036476 FDA UDI
FDA Product Code
CKG FDA UDI
GMDN Term
Adrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1025 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 4 Milliliter FDA UDI
Total Volume — 2 Milliliter FDA UDI
Total Volume — 2.7 Milliliter FDA UDI
Total Volume — 20 Milliliter FDA UDI
Total Volume — 30 Milliliter FDA UDI
Total Volume — 15.5 Milliliter FDA UDI

Category: Adrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA)

ACTH (Adrenocorticotropic Hormone) ELISA by DRG International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Adrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA).

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 33f4997a-19f8-468f-b74e-788ce515e933 36 fields · synced Jun 1, 2026