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DBC Total Estrogens ELISA

FDA UDIEUDAMED

Class I (US FDA UDI)

by Diagnostics Biochem Canada Inc

Identity

Trade Name
DBC Total Estrogens ELISA FDA UDI
Generic Name
Total estrogen (oestrogen) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
For the quantitative measurement of Total Estrogens in human serum by an ELISA (Enzyme-Linked Immunosorbent Assay). For in vitro diagnostic use. FDA UDI
Model / Reference
CAN-E-630-8PK FDA UDI
Description
For the quantitative measurement of Total Estrogens in human serum by an ELISA (Enzyme-Linked Immunosorbent Assay). For in vitro diagnostic use. FDA UDI

Identifiers

Catalog Number
CAN-E-630-8PK FDA UDI
Primary DI / UDI-DI
B261CANE6308PK0 FDA UDI
FDA Product Code
JMD FDA UDI
GMDN Term
Total estrogen (oestrogen) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1275 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: Total estrogen (oestrogen) IVD, kit, enzyme immunoassay (EIA)

DBC Total Estrogens 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 Total estrogen (oestrogen) 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 120db5f8-18a8-4887-b1f4-cf3214a209c8 36 fields · synced Jun 17, 2026
  • EUDAMED 1 fields · synced Jun 3, 2026