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QMedix™

FDA UDI

Class II (US FDA UDI)

by Diagnostic Automation, Inc.

Identity

Trade Name
QMedix™ FDA UDI
Generic Name
Thyroid stimulating hormone (TSH) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
QMedix™TSH ELISA This test is intended to be used for the quantitative measurement of thyroid stimulating hormone (TSH) in a clinical specimen, using an enzyme immunoassay (EIA) method. FDA UDI
Model / Reference
DACD3122-15 FDA UDI
Description
QMedix™TSH ELISA This test is intended to be used for the quantitative measurement of thyroid stimulating hormone (TSH) in a clinical specimen, using an enzyme immunoassay (EIA) method. FDA UDI

Identifiers

Catalog Number
3122-15 FDA UDI
Primary DI / UDI-DI
00850054026439 FDA UDI
FDA Product Code
JLW FDA UDI
GMDN Term
Thyroid stimulating hormone (TSH) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1690 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

No

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

No

FDA UDI

Category: Thyroid stimulating hormone (TSH) IVD, kit, enzyme immunoassay (EIA)

QMedix™ by Diagnostic Automation, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thyroid stimulating hormone (TSH) 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 b952f0a6-fb08-4d92-b270-69f29ceb91ed 37 fields · synced Jun 8, 2026