Didas Vacuum Blood Collection System (Sterilization) - Taiwan Registration e3b2b0d3c0b8f35922b22153c4e4674f
Access comprehensive regulatory information for Didas Vacuum Blood Collection System (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e3b2b0d3c0b8f35922b22153c4e4674f and manufactured by ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, 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.
Device Details
Product Details
Limited to the first level identification range of the "Vacuum Blood Collection System (B.9125)" of the Measures for the Classification and Grading Management of Medical Equipment.
B Hematology, pathology, and genetics
B.9125 Vacuum blood collection system
Input;; QMS/QSD;; Chinese goods
Dates and Status
Jul 24, 2017
Jul 24, 2027

