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Anti-Thyroglobulin (Anti-Tg) ELISA

FDA UDI

Class II (US FDA UDI)

by DRG Instruments Gesellschaft mit beschränkter Haftung

Identity

Trade Name
Anti-Thyroglobulin (Anti-Tg) ELISA FDA UDI
Generic Name
Multiple thyroid antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
The Quantitative Determination of Thyroglobulin (Tg) Autoantibodies in Human Serum or Plasma by a Microplate Enzyme Immunoassay, Colorimetric. FDA UDI
Model / Reference
EIA-4110 FDA UDI
Description
The Quantitative Determination of Thyroglobulin (Tg) Autoantibodies in Human Serum or Plasma by a Microplate Enzyme Immunoassay, Colorimetric. FDA UDI

Identifiers

Catalog Number
EIA-4110 FDA UDI
Primary DI / UDI-DI
04048474041101 FDA UDI
510(k) Number
K971835 FDA UDI
FDA Product Code
DDC FDA UDI
GMDN Term
Multiple thyroid antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5870 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

No

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 antibody IVD, kit, enzyme immunoassay (EIA)

Anti-Thyroglobulin (Anti-Tg) ELISA by DRG Instruments Gesellschaft mit beschränkter Haftung — Class II — FDA UDI — listed in FDA GUDID

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 065d566f-e099-4bbe-b617-043c4a70c8b0 37 fields · synced May 30, 2026