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Estrone-RIA-CT

FDA UDI

Class I (US FDA UDI)

by Diasource Immunoassays, S.A.

Identity

Trade Name
Estrone-RIA-CT FDA UDI
Generic Name
Estrone (oestrone) IVD, kit, radioimmunoassay FDA UDI
Device Name
Estrone-RIA-CT FDA UDI
Model / Reference
KIPI9100 FDA UDI
Description
Estrone-RIA-CT FDA UDI

Identifiers

Primary DI / UDI-DI
05400569000674 FDA UDI
FDA Product Code
CGF FDA UDI
GMDN Term
Estrone (oestrone) IVD, kit, radioimmunoassay 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Estrone (oestrone) IVD, kit, radioimmunoassay

Estrone-RIA-CT by Diasource Immunoassays, S.A. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Estrone (oestrone) IVD, kit, radioimmunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bdb2d164-467f-47cc-bb95-4d77d7d21071 33 fields · synced May 30, 2026