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OYE Rapid Pregnancy Test Series - Taiwan Registration 02171f4ab94d66c0c103164229ba1da5

Access comprehensive regulatory information for OYE Rapid Pregnancy Test Series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 02171f4ab94d66c0c103164229ba1da5 and manufactured by Ouye Pharmaceutical Co., Ltd.; Dongyao Biotechnology Co., Ltd. The authorized representative in Taiwan is OU-YEH 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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02171f4ab94d66c0c103164229ba1da5
Registration Details
Taiwan FDA Registration: 02171f4ab94d66c0c103164229ba1da5
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Device Details

OYE Rapid Pregnancy Test Series
TW: ๆญๆฅญๅฟซ้€Ÿ้ฉ—ๅญ•ๆธฌ่ฉฆ็ณปๅˆ—
Risk Class 2

Registration Details

02171f4ab94d66c0c103164229ba1da5

Company Information

Product Details

The urine is tested for whether it contains human chorionic gonadotropin (HCG).

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

Contract manufacturing;; Domestic

Dates and Status

Sep 30, 2017

Sep 28, 2025