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CJ Rapitest PSA test kit - Taiwan Registration ae680624f062231c967512727b553602

Access comprehensive regulatory information for CJ Rapitest PSA test kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae680624f062231c967512727b553602 and manufactured by Qizhe Biotechnology Co., Ltd. The authorized representative in Taiwan is Qizhe 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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ae680624f062231c967512727b553602
Registration Details
Taiwan FDA Registration: ae680624f062231c967512727b553602
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Device Details

CJ Rapitest PSA test kit
TW: ๅ•Ÿๅ“ฒ้€Ÿๆธฌๅฎถๅ‰ๅˆ—่…บ็‰น็•ฐๆ€งๆŠ—ๅŽŸๆชขๆธฌ่ฉฆๅŠ‘็ต„
Risk Class 2
MD

Registration Details

ae680624f062231c967512727b553602

Ministry of Health Medical Device Manufacturing No. 005599

Company Information

Taiwan, Province of China

Product Details

Qualitative detection of prostate-specific antigen (PSA) in human serum.

C Immunology and microbiology devices

C6010 Tumor-associated antigen immunoassay system

Produced in Taiwan, China

Dates and Status

Apr 14, 2017

Apr 14, 2022