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"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..

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e7f8ed299e50234b6328d84f0c396877
Registration Details
Taiwan FDA Registration: e7f8ed299e50234b6328d84f0c396877
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Device Details

"Yongkang" single-use venous blood collection needle
TW: “永康”一次性使用靜脈採血針
Risk Class 2

Registration Details

e7f8ed299e50234b6328d84f0c396877

DHA09200091302

Company Information

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