← Back to catalogue

TSH Receptor Autoantibody ELISA

FDA UDI

Class II (US FDA UDI)

by DRG Instruments Gesellschaft mit beschränkter Haftung

Identity

Trade Name
TSH Receptor Autoantibody ELISA FDA UDI
Generic Name
Thyroid stimulating hormone receptor (TSHR) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
The TSH receptor (TSHR) autoantibody (TRAb) ELISA kit is intended for use by professional persons only for the quantitative determination of TRAb in human serum FDA UDI
Model / Reference
EIA-3369 FDA UDI
Description
The TSH receptor (TSHR) autoantibody (TRAb) ELISA kit is intended for use by professional persons only for the quantitative determination of TRAb in human serum FDA UDI

Identifiers

Catalog Number
EIA-3369 FDA UDI
Primary DI / UDI-DI
04048474033694 FDA UDI
510(k) Number
K032134 FDA UDI
FDA Product Code
JZO FDA UDI
GMDN Term
Thyroid stimulating hormone receptor (TSHR) 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: Thyroid stimulating hormone receptor (TSHR) antibody IVD, kit, enzyme immunoassay (EIA)

TSH Receptor Autoantibody ELISA by DRG Instruments Gesellschaft mit beschränkter Haftung — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Thyroid stimulating hormone receptor (TSHR) antibody IVD, kit, enzyme immunoassay (EIA).

Cleared under the same submission

K032134 also covers:

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

Manufacturer
DRG Instruments Gesellschaft mit beschränkter Haftung

Sources (1)

  • FDA UDI 0366d7bf-2048-4408-a26a-d3dc2769b91a 37 fields · synced May 30, 2026