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"Sudi" Ovulation Rapid Test Reagent (Unsterilized) - Taiwan Registration 1c6cc0a3915ae3b27a27e20a9eaecf6c

Access comprehensive regulatory information for "Sudi" Ovulation Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1c6cc0a3915ae3b27a27e20a9eaecf6c and manufactured by STANDARD DIAGNOSTICS, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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1c6cc0a3915ae3b27a27e20a9eaecf6c
Registration Details
Taiwan FDA Registration: 1c6cc0a3915ae3b27a27e20a9eaecf6c
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Device Details

"Sudi" Ovulation Rapid Test Reagent (Unsterilized)
TW: โ€œ้€Ÿๅธโ€ๆŽ’ๅตๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

1c6cc0a3915ae3b27a27e20a9eaecf6c

DHA04400907902

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the "luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Equipment.

A Clinical chemistry and clinical toxicology

A.1485 Progesterone testing system

import

Dates and Status

Aug 12, 2010

Aug 12, 2020

Jul 15, 2022

Cancellation Information

Logged out

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