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Free Triiodothyronine (fT3) ELISA

FDA UDI

Class II (US FDA UDI)

by DRG Instruments Gesellschaft mit beschränkter Haftung

Identity

Trade Name
Free Triiodothyronine (fT3) ELISA FDA UDI
Generic Name
Multiple thyroid marker IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
For the quantitative determination of Free Triiodothyronine (fT3) concentration in human serum. FDA UDI
Model / Reference
EIA-2385 FDA UDI
Description
For the quantitative determination of Free Triiodothyronine (fT3) concentration in human serum. FDA UDI

Identifiers

Catalog Number
EIA-2385 FDA UDI
Primary DI / UDI-DI
04048474023855 FDA UDI
FDA Product Code
CDP FDA UDI
GMDN Term
Multiple thyroid marker IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1710 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: Multiple thyroid marker IVD, kit, enzyme immunoassay (EIA)

Free Triiodothyronine (fT3) ELISA by DRG Instruments Gesellschaft mit beschränkter Haftung — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Multiple thyroid marker 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 49cf1e0c-8187-4c81-9ac7-1b0ecac04ab8 36 fields · synced May 30, 2026