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DBC Free Testosterone ELISA

FDA UDI

Class I (US FDA UDI)

by Diagnostics Biochem Canada Inc

Identity

Trade Name
DBC Free Testosterone ELISA FDA UDI
Generic Name
Free testosterone IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
For the direct quantitative determination of Free Testosterone by an enzyme immunoassay in human serum. For in vitro diagnostic use. FDA UDI
Model / Reference
CAN-FTE-260LC8 FDA UDI
Description
For the direct quantitative determination of Free Testosterone by an enzyme immunoassay in human serum. For in vitro diagnostic use. FDA UDI

Identifiers

Catalog Number
CAN-FTE-260LC8 FDA UDI
Primary DI / UDI-DI
B261CANFTE260LC80 FDA UDI
510(k) Number
K030730 FDA UDI
FDA Product Code
CDZ FDA UDI
GMDN Term
Free testosterone IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1680 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Free testosterone IVD, kit, enzyme immunoassay (EIA)

DBC Free Testosterone ELISA by Diagnostics Biochem Canada Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Free testosterone 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 a19f7c8b-1e9d-49db-a815-24deb54c68e2 37 fields · synced Jun 8, 2026