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"Biosen Webster" Ottari high-density mapping catheter - Taiwan Registration 21a225e53350b183e33fb33e886ff857

Access comprehensive regulatory information for "Biosen Webster" Ottari high-density mapping catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21a225e53350b183e33fb33e886ff857 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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21a225e53350b183e33fb33e886ff857
Registration Details
Taiwan FDA Registration: 21a225e53350b183e33fb33e886ff857
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Device Details

"Biosen Webster" Ottari high-density mapping catheter
TW: โ€œ็™พๆญๆฃฎๅ‰ไผฏๅธ็‰นโ€ ๆญๅก”็‘ž้ซ˜ๅฏ†ๅบฆๆจ™ๆธฌๅฐŽ็ฎก
Risk Class 2

Registration Details

21a225e53350b183e33fb33e886ff857

DHA05603577302

Company Information

Mexico;;United States

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1220 ้›ปๆฅต่จ˜้Œ„ๅฐŽ็ฎกๆˆ–้›ปๆฅต่จ˜้Œ„ๆŽข้ ญ

import

Dates and Status

Aug 30, 2022

Aug 30, 2027