Pure Global

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
e3b2b0d3c0b8f35922b22153c4e4674f
Registration Details
Taiwan FDA Registration: e3b2b0d3c0b8f35922b22153c4e4674f
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Didas Vacuum Blood Collection System (Sterilization)
TW: "่ซฆ้”ๆ€" ็œŸ็ฉบ่ก€ๆถฒๆ”ถ้›†็ณป็ตฑ (ๆป…่Œ)
Risk Class 1

Registration Details

e3b2b0d3c0b8f35922b22153c4e4674f

DHA09600315701

Company Information

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