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DBC Free Estriol ELISA

FDA UDIEUDAMED

Class I (US FDA UDI)

by Diagnostics Biochem Canada Inc

Identity

Trade Name
DBC Free Estriol ELISA FDA UDI
Generic Name
Free estriol (oestriol) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
For the quantitative measurement of Free Estriol in human serum by an ELISA (Enzyme-Linked Immunosorbent Assay). For in vitro diagnostic use. FDA UDI
Model / Reference
CAN-E-640 FDA UDI
Description
For the quantitative measurement of Free Estriol in human serum by an ELISA (Enzyme-Linked Immunosorbent Assay). For in vitro diagnostic use. FDA UDI

Identifiers

Catalog Number
CAN-E-640 FDA UDI
Primary DI / UDI-DI
B261CANE6400 FDA UDI
FDA Product Code
CGI FDA UDI
GMDN Term
Free estriol (oestriol) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1265 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Free estriol (oestriol) IVD, kit, enzyme immunoassay (EIA)

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

Similar devices

Also classified as Free estriol (oestriol) IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 72adf2f7-1325-454a-9593-8788543b5b8a 36 fields · synced Jun 17, 2026
  • EUDAMED 1 fields · synced Jun 1, 2026