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Bafang rapid pregnancy test reagent - Taiwan Registration 0e9705cfde3e5c5d0354cd37589b10d9

Access comprehensive regulatory information for Bafang rapid 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 0e9705cfde3e5c5d0354cd37589b10d9 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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0e9705cfde3e5c5d0354cd37589b10d9
Registration Details
Taiwan FDA Registration: 0e9705cfde3e5c5d0354cd37589b10d9
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Device Details

Bafang rapid pregnancy test reagent
TW: ๅ…ซๆ–นๅฟซ้€Ÿ้ฉ—ๅญ•่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

0e9705cfde3e5c5d0354cd37589b10d9

DHY00500216702

Company Information

Taiwan, Province of China

Product Details

Immunochromatography was used to qualitatively detect human placental chorionic gonadal hormone (threshold 25 mIU/mL) in urine.

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

Domestic

Dates and Status

Aug 09, 2006

Aug 09, 2011

Oct 25, 2012

Cancellation Information

Logged out

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