Pure Global

"Luci" ureteral stent - Taiwan Registration 0626700459845761fe1aa4df974c1591

Access comprehensive regulatory information for "Luci" ureteral stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0626700459845761fe1aa4df974c1591 and manufactured by Teleflex Medical; Arrow International CR, a.s. Branch in Žďár nad Sázavou. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN 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
0626700459845761fe1aa4df974c1591
Registration Details
Taiwan FDA Registration: 0626700459845761fe1aa4df974c1591
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Luci" ureteral stent
TW: “路希”輸尿管支架
Risk Class 2

Registration Details

0626700459845761fe1aa4df974c1591

DHA05603222100

Company Information

Product Details

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

H Gastroenterology and urology

H.4620 Urinary Catheter Stent

Input;; Contract manufacturing

Dates and Status

Jan 23, 2019

Jan 23, 2029