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Sunflower rapid pregnancy test reagent series - Taiwan Registration 17fe970e383d1e4b7e33bd7927e3b83f

Access comprehensive regulatory information for Sunflower rapid pregnancy test reagent series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17fe970e383d1e4b7e33bd7927e3b83f and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is HAN CHUAN MEDICAL MATERIAL BIO-TEC CO., LTD..

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17fe970e383d1e4b7e33bd7927e3b83f
Registration Details
Taiwan FDA Registration: 17fe970e383d1e4b7e33bd7927e3b83f
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Device Details

Sunflower rapid pregnancy test reagent series
TW: ๅ‘ๆ—ฅ่‘ตๅฟซ้€Ÿ้ฉ—ๅญ•่ฉฆๅŠ‘็ณปๅˆ—
Risk Class 2

Registration Details

17fe970e383d1e4b7e33bd7927e3b83f

DHY00500359107

Company Information

Taiwan, Province of China

Product Details

Serum or urine is tested for human chorionic gonadotropin (HCG). The change in efficacy (removal of serum source and addition of non-specialist use) is the qualitative test of urine for human chorionic gonadotropin (HCG).

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

Domestic;; Contract manufacturing

Dates and Status

Feb 21, 2012

Sep 28, 2025