"Yongkang" single-use venous blood collection needle - Taiwan Registration e7f8ed299e50234b6328d84f0c396877
Access comprehensive regulatory information for "Yongkang" single-use venous blood collection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e7f8ed299e50234b6328d84f0c396877 and manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO.,LTD.;; 永康醫材科技股份有限公司. The authorized representative in Taiwan is YUNG KANG MEDICAL DEVICE TECHNOLOGY 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.
Device Details
Registration Details
e7f8ed299e50234b6328d84f0c396877
DHA09200091302
Product Details
For details, it is Chinese approved copy of the imitation order
J General hospital and personal use equipment
J.5570 Subcutaneous single-chamber needle
Chinese goods;; Contract manufacturing;; input
Dates and Status
May 16, 2018
May 16, 2023

