Pure Global

“KDL” SCALP VEIN SET - Taiwan Registration 0a7f609289f75b8366c97e48fda4fbbe

Access comprehensive regulatory information for “KDL” SCALP VEIN SET in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0a7f609289f75b8366c97e48fda4fbbe and manufactured by Zhejiang Kindly Medical Devices Co., Ltd.. The authorized representative in Taiwan is KENYEN INTERNATIONAL INC..

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
0a7f609289f75b8366c97e48fda4fbbe
Registration Details
Taiwan FDA Registration: 0a7f609289f75b8366c97e48fda4fbbe
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“KDL” SCALP VEIN SET
TW: “康德萊”頭皮針
Risk Class 2
MD

Registration Details

0a7f609289f75b8366c97e48fda4fbbe

Ministry of Health Medical Device Land Transport No. 000585

DHA09200058501

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

J General hospital and personal use equipment

J5440 Intravascular infusion sleeve

Imported from abroad; Made in China

Dates and Status

Mar 19, 2014

Mar 19, 2024