Dual-function inspection system for automatic film withdrawal (unsterilized) - Taiwan Registration a4b2e767ebebd5f5399d4fed4c854a54
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 a4b2e767ebebd5f5399d4fed4c854a54 and manufactured by Qinli Biotechnology Co., Ltd. new tree factory. 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 North Plant, 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
It is limited to the first level of the classification and grading management measures for medical devices, "Quality Control Materials (Analytical and Non-Analytical) (A.1660)", "Uric Acid Test System (A.1775)", "Manual Instruments for General Surgery (I.4800)", and "Cholesterol (Total) Test System (A.1175)".
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
QMS/QSD;; ๅ็ข
Dates and Status
May 25, 2017
May 25, 2027