Pure Global

"Bonthe" intravascular guide steel wire - Taiwan Registration 5bf09f2778189381b9ee78dc9782e827

Access comprehensive regulatory information for "Bonthe" intravascular guide steel wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5bf09f2778189381b9ee78dc9782e827 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
5bf09f2778189381b9ee78dc9782e827
Registration Details
Taiwan FDA Registration: 5bf09f2778189381b9ee78dc9782e827
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Bonthe" intravascular guide steel wire
TW: โ€œ้‚ฆ็‰นโ€่ก€็ฎกๅ…งๅผ•ๅฐŽ้‹ผ็ทš
Risk Class 2

Registration Details

5bf09f2778189381b9ee78dc9782e827

DHY00500353701

Company Information

Taiwan, Province of China

Product Details

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

E Cardiovascular Medicine Science

E.1330 Catheter Guide Wires

Domestic

Dates and Status

Apr 12, 2012

Apr 12, 2027