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Kim Caisha Rapid Pregnancy Test Pen - Taiwan Registration 9a7e5d25d25dee05e62396a719e3a7ba

Access comprehensive regulatory information for Kim Caisha Rapid Pregnancy Test Pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9a7e5d25d25dee05e62396a719e3a7ba and manufactured by The first factory of Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is Xinghai Pharmaceutical 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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9a7e5d25d25dee05e62396a719e3a7ba
Registration Details
Taiwan FDA Registration: 9a7e5d25d25dee05e62396a719e3a7ba
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Device Details

Kim Caisha Rapid Pregnancy Test Pen
TW: ้‡‘้‡‡ๅธ›่ŽŽๅฟซ้€Ÿ้ฉ—ๅญ•่ฉฆๅŠ‘็ญ†
Risk Class 2
Cancelled

Registration Details

9a7e5d25d25dee05e62396a719e3a7ba

DHY00500305101

Company Information

Taiwan, Province of China

Product Details

The concentration of hCG in human urine is measured.

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

Domestic

Dates and Status

Jun 30, 2010

Dec 12, 2020

Jun 16, 2022

Cancellation Information

Logged out

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