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Fusheng rapid pregnancy test reagent - Taiwan Registration 8f7174e24defc333144fd10cc920305d

Access comprehensive regulatory information for Fusheng 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 8f7174e24defc333144fd10cc920305d and manufactured by HANGZHOU BIOTEST BIOTECH CO., LTD.. The authorized representative in Taiwan is FORTUNE CROESUS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Formosa Biomedical Technology Co., Ltd. Yilan Factory;; Fusheng International Trading Co., Ltd, and 1 recent registrations in the same category. 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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8f7174e24defc333144fd10cc920305d
Registration Details
Taiwan FDA Registration: 8f7174e24defc333144fd10cc920305d
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Device Details

Fusheng rapid pregnancy test reagent
TW: ๅฏŒ่–ๅฟซ้€Ÿ้ฉ—ๅญ•ๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 2

Registration Details

8f7174e24defc333144fd10cc920305d

DHA09200061701

Company Information

Product Details

This reagent uses rapid immunochromatography to detect human chorionic gonadotropin (HCG) in urine samples to detect pregnancy early.

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

Chinese goods;; input

Dates and Status

Jun 27, 2014

Jun 27, 2029

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