Dual-function inspection system for automatic film withdrawal (unsterilized) - Taiwan Registration 595a2f6b3ee92b67d8d8c27ab0858ed5
Access comprehensive regulatory information for Dual-function inspection system for automatic film withdrawal (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 595a2f6b3ee92b67d8d8c27ab0858ed5 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, 1 companies making similar products including Qinli Biotechnology Co., Ltd. new tree factory, and 1 recent registrations in the same category. 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.
Device Details
Product Details
Limited to the classification and grading management of medical devices, "cholesterol (total) test system (A.1175), uric acid test system (A.1775)", "quality control materials (analytical and non-analytical) (A.1660)", "manual instruments for general surgery (I.4800)" first grade identification range.
A Clinical chemistry and clinical toxicology
A.1775 Uric acid test system;; A.1660 Grade Material (Analysis Material Non-Analysis);; A.1175 ่ฝๅบ้(็ธฝ้)่ฉฆ้ฉ็ณป็ตฑ
ๅ็ข;; QMS/QSD
Dates and Status
Oct 12, 2022
Oct 12, 2027