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Whole Valley Precision Pregnancy Test Reagent - Taiwan Registration 7dd2163ad747403da99f590a26e5ba94

Access comprehensive regulatory information for Whole Valley Precision Pregnancy Test Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7dd2163ad747403da99f590a26e5ba94 and manufactured by Lianshang Biotechnology Co., Ltd. Wugu Factory. The authorized representative in Taiwan is Whole Valley Biotechnology Co., Ltd.

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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7dd2163ad747403da99f590a26e5ba94
Registration Details
Taiwan FDA Registration: 7dd2163ad747403da99f590a26e5ba94
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Device Details

Whole Valley Precision Pregnancy Test Reagent
TW: ๅ…จ่ฐท็ฒพๆบ–้ฉ—ๅญ•่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

7dd2163ad747403da99f590a26e5ba94

DHY00500216804

Company Information

Taiwan, Province of China

Product Details

Rapid immunoassay was used to detect human placental chorionic gonadal hormone in urine.

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

Domestic

Dates and Status

Aug 10, 2006

Aug 10, 2011

Oct 25, 2012

Cancellation Information

Logged out

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