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LOVECARE HCG RAPID TEST - Taiwan Registration bafc3f8970b47834d882d3a668f4a0dc

Access comprehensive regulatory information for LOVECARE HCG RAPID TEST in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bafc3f8970b47834d882d3a668f4a0dc and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is JIEDUO ENTERPRISE CO., LTD..

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bafc3f8970b47834d882d3a668f4a0dc
Registration Details
Taiwan FDA Registration: bafc3f8970b47834d882d3a668f4a0dc
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Device Details

LOVECARE HCG RAPID TEST
TW: ๅฉ•ๆœตๅฟซ้€Ÿ้ฉ—ๅญ•่ฉฆๅŠ‘็ณป็ตฑ
Risk Class 2
MD

Registration Details

bafc3f8970b47834d882d3a668f4a0dc

Department of Health Medical Device Manufacturing No. 003508

DHY00500350807

Company Information

Taiwan, Province of China

Product Details

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

A1155 Human chorionic gonadotropin test system

Produced in Taiwan, China; Contract manufacturing

Dates and Status

Jan 18, 2012

Sep 28, 2025