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“BIOTEQ”Micro Catheter Kit - Taiwan Registration d2721577d43065487980731e51f1da5c

Access comprehensive regulatory information for “BIOTEQ”Micro Catheter Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2721577d43065487980731e51f1da5c 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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d2721577d43065487980731e51f1da5c
Registration Details
Taiwan FDA Registration: d2721577d43065487980731e51f1da5c
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Device Details

“BIOTEQ”Micro Catheter Kit
TW: “邦特”微導管套組
Risk Class 2
MD

Registration Details

d2721577d43065487980731e51f1da5c

Ministry of Health Medical Device Manufacturing No. 007661

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E1250 Percutaneous catheter

Produced in Taiwan, China

Dates and Status

Jul 25, 2022

Jul 25, 2027