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“BONTEQ” Angiographic Catheters - Taiwan Registration df42dbbfbd5aae696a17427d8e881920

Access comprehensive regulatory information for “BONTEQ” Angiographic Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df42dbbfbd5aae696a17427d8e881920 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.

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Registration Details
Taiwan FDA Registration: df42dbbfbd5aae696a17427d8e881920
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Device Details

“BONTEQ” Angiographic Catheters
TW: “全保”血管攝影導管
Risk Class 2
MD

Registration Details

df42dbbfbd5aae696a17427d8e881920

Ministry of Health Medical Device Manufacturing No. 006150

Company Information

Taiwan, Province of China

Product Details

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

E Cardiovascular devices

E1200 Diagnostic endovascular catheter

Produced in Taiwan, China

Dates and Status

Sep 05, 2018

Sep 04, 2026