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“Baylis” TorFlex Transseptal Guiding Sheath - Taiwan Registration e94755dd3444854a37a2b61e171191d5

Access comprehensive regulatory information for “Baylis” TorFlex Transseptal Guiding Sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e94755dd3444854a37a2b61e171191d5 and manufactured by BAYLIS MEDICAL COMPANY INC.. The authorized representative in Taiwan is WIN CHAMP MEDICAL CO., 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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e94755dd3444854a37a2b61e171191d5
Registration Details
Taiwan FDA Registration: e94755dd3444854a37a2b61e171191d5
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Device Details

“Baylis” TorFlex Transseptal Guiding Sheath
TW: “拜利斯”拖菲斯心房中膈導引鞘
Risk Class 2
MD

Registration Details

e94755dd3444854a37a2b61e171191d5

Ministry of Health Medical Device Import No. 028236

DHA05602823608

Company Information

Canada

Product Details

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

E Cardiovascular devices

E1340 Catheter Guide

Imported from abroad

Dates and Status

Feb 17, 2016

Feb 17, 2026