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Estrone ELISA

FDA UDI

Class I (US FDA UDI)

by IBL America

Identity

Trade Name
Estrone ELISA FDA UDI
Generic Name
Estrone (oestrone) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
For the quantitative measurement of Estrone in human serum by an ELISA (Enzyme-Linked Immunosorbent Assay). FDA UDI
Model / Reference
IB59105 FDA UDI
Description
For the quantitative measurement of Estrone in human serum by an ELISA (Enzyme-Linked Immunosorbent Assay). FDA UDI

Identifiers

Catalog Number
IB59105 FDA UDI
Primary DI / UDI-DI
B652IB59105 FDA UDI
FDA Product Code
CGF FDA UDI
GMDN Term
Estrone (oestrone) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1280 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: Estrone (oestrone) IVD, kit, enzyme immunoassay (EIA)

Estrone ELISA by IBL America — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Estrone (oestrone) IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
IBL America

Sources (1)

  • FDA UDI e4b720f0-c4eb-4472-b815-1f59309a9dac 36 fields · synced May 30, 2026