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"Biosen Webster" Cadofiseo double guide sheath tube - Taiwan Registration b0b0bf18afafc818c6b192f20044d912

Access comprehensive regulatory information for "Biosen Webster" Cadofiseo double guide sheath tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0b0bf18afafc818c6b192f20044d912 and manufactured by Biosense Webster, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..

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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b0b0bf18afafc818c6b192f20044d912
Registration Details
Taiwan FDA Registration: b0b0bf18afafc818c6b192f20044d912
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Device Details

"Biosen Webster" Cadofiseo double guide sheath tube
TW: โ€œ็™พๆญๆฃฎๅ‰ไผฏๅธ็‰นโ€ๅกๅคš่ฒปๆ–ฏๆญ้›™ๅ‘ๅฐŽๅผ•้ž˜็ฎก
Risk Class 2

Registration Details

b0b0bf18afafc818c6b192f20044d912

DHA05603357501

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1340 Catheter Introducers

import

Dates and Status

Apr 29, 2020

Apr 29, 2025