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17ohp Ria Ct

FDA UDI

Class I (US FDA UDI)

by Diasource Immunoassays, S.A.

Identity

Trade Name
17OHP RIA CT FDA UDI
Generic Name
17-Hydroxyprogesterone IVD, kit, radioimmunoassay FDA UDI
Device Name
17OHP RIA CT FDA UDI
Model / Reference
KIP1409 FDA UDI
Description
17OHP RIA CT FDA UDI

Identifiers

Primary DI / UDI-DI
05400569000476 FDA UDI
FDA Product Code
JLX FDA UDI
GMDN Term
17-Hydroxyprogesterone IVD, kit, radioimmunoassay FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1395 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: 17-Hydroxyprogesterone IVD, kit, radioimmunoassay

17ohp Ria Ct by Diasource Immunoassays, S.A. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as 17-Hydroxyprogesterone IVD, kit, radioimmunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diasource Immunoassays, S.A.

Sources (1)

  • FDA UDI 062a4e6a-4a6d-4d5f-bc75-cc2a2d768575 33 fields · synced May 30, 2026