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Baijie heme quality solution (unsterilized) - Taiwan Registration 0056c33a7b8b57ae7f6fdb6bd0d99191

Access comprehensive regulatory information for Baijie heme quality solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0056c33a7b8b57ae7f6fdb6bd0d99191 and manufactured by Qinli Biotechnology Co., Ltd. New North Plant. The authorized representative in Taiwan is GENERAL LIFE 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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0056c33a7b8b57ae7f6fdb6bd0d99191
Registration Details
Taiwan FDA Registration: 0056c33a7b8b57ae7f6fdb6bd0d99191
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Device Details

Baijie heme quality solution (unsterilized)
TW: ็™พๆท่ก€็ด…็ด ๅ“็ฎกๆถฒ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

0056c33a7b8b57ae7f6fdb6bd0d99191

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.

A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical)

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Apr 20, 2022

Apr 20, 2027