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“BIOTEQ” Drainage Catheter (Long-term Type) - Taiwan Registration 192b4d333a2f61b95b27a0230db3ff34

Access comprehensive regulatory information for “BIOTEQ” Drainage Catheter (Long-term Type) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 192b4d333a2f61b95b27a0230db3ff34 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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192b4d333a2f61b95b27a0230db3ff34
Registration Details
Taiwan FDA Registration: 192b4d333a2f61b95b27a0230db3ff34
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Device Details

“BIOTEQ” Drainage Catheter (Long-term Type)
TW: “邦特”引流導管(長效型)
Risk Class 2
MD

Registration Details

192b4d333a2f61b95b27a0230db3ff34

Ministry of Health Medical Device Manufacturing No. 006325

Company Information

Taiwan, Province of China

Product Details

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

H Gastroenterology-urology devices

H5010 Bile ductal catheters and their accessories

Produced in Taiwan, China

Dates and Status

Mar 19, 2019

Mar 19, 2029