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"Edward" Ovulation Rapid Test Reagent (Unsterilized) - Taiwan Registration 3723508e7eb91a341dbaf2baa3247d6a

Access comprehensive regulatory information for "Edward" 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 3723508e7eb91a341dbaf2baa3247d6a and manufactured by AIDE DIAGNOSTIC CO., LTD.. The authorized representative in Taiwan is WinBaby Co..

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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3723508e7eb91a341dbaf2baa3247d6a
Registration Details
Taiwan FDA Registration: 3723508e7eb91a341dbaf2baa3247d6a
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Device Details

"Edward" Ovulation Rapid Test Reagent (Unsterilized)
TW: "่‰พๅพท" ๆŽ’ๅตๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

3723508e7eb91a341dbaf2baa3247d6a

DHA09600284705

Company Information

China

Product Details

Limited to the first level recognition range of the "Luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A.1485 Progesterone testing system

Input;; Chinese goods

Dates and Status

Sep 05, 2016

Sep 05, 2021

Sep 19, 2023

Cancellation Information

Logged out

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