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.
Device Details
Registration Details
7dd2163ad747403da99f590a26e5ba94
DHY00500216804
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
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