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Speedy pregnancy human chorionic gonadotropin test system - Taiwan Registration ddf3e8d8f107d9ed1c67ff42a74b9dc3

Access comprehensive regulatory information for Speedy pregnancy human chorionic gonadotropin test system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ddf3e8d8f107d9ed1c67ff42a74b9dc3 and manufactured by IND DIAGNOSTIC INC.. The authorized representative in Taiwan is SCIENSER INTERNATIONAL INC..

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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ddf3e8d8f107d9ed1c67ff42a74b9dc3
Registration Details
Taiwan FDA Registration: ddf3e8d8f107d9ed1c67ff42a74b9dc3
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Device Details

Speedy pregnancy human chorionic gonadotropin test system
TW: ้€Ÿ็Ÿฅๅญ•ไบบ้กž็ตจๆฏ›่†œไฟƒๆ€ง่…บๆฟ€็ด ่ฉฆ้ฉ—็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

ddf3e8d8f107d9ed1c67ff42a74b9dc3

DHA00601222500

Company Information

Canada

Product Details

The results of the visual inspection can determine whether you are pregnant.

A Clinical chemistry and clinical toxicology

import

Dates and Status

Sep 06, 2005

Sep 06, 2015

Aug 09, 2018

Cancellation Information

Logged out

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