Pure Global

“BONTEQ” Ureteral Stent Set - Taiwan Registration d405039d2756a1c6562300d66a9d83c6

Access comprehensive regulatory information for “BONTEQ” Ureteral Stent Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d405039d2756a1c6562300d66a9d83c6 and manufactured by Bonte Biotechnology Co., Ltd. Yilan Plant 2. The authorized representative in Taiwan is BIOTEQUE CORPORATION.

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
d405039d2756a1c6562300d66a9d83c6
Registration Details
Taiwan FDA Registration: d405039d2756a1c6562300d66a9d83c6
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“BONTEQ” Ureteral Stent Set
TW: “全保”輸尿管導管組
Risk Class 2
MD

Registration Details

d405039d2756a1c6562300d66a9d83c6

Ministry of Health Medical Device Manufacturing No. 006167

Company Information

Taiwan, Province of China

Product Details

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

H Gastroenterology-urology devices

H4620 Ureteral stents

Produced in Taiwan, China

Dates and Status

Jul 30, 2018

Jun 10, 2027