Taiwan FDA registration e7f8ed299e50234b6328d84f0c396877

"Yongkang" single-use venous blood collection needle

TW: “永康”一次性使用靜脈採血針

Taiwan·Risk Class 2·GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO.,LTD.;; 永康醫材科技股份有限公司·Registered May 16, 2018 – May 16, 2023Expired

Registration details

Analysis ID: e7f8ed299e50234b6328d84f0c396877
Customs Code: DHA09200091302

Company information

Manufacturer: GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO.,LTD.;; 永康醫材科技股份有限公司
Manufacturer Country: Taiwan, Province of China;;China
Authorized Representative: YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5570 Subcutaneous single-chamber needle
Import Information: Chinese goods;; Contract manufacturing;; input

Dates and status

Registration Date: May 16, 2018
Expiry Date: May 16, 2023

About this record

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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