Pure Global

“BIOTRONIK”Senovo Bi-Flex Steerable Guiding Sheath - Taiwan Registration a781428fe0c2f224a868ac541450c572

Access comprehensive regulatory information for “BIOTRONIK”Senovo Bi-Flex Steerable 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 a781428fe0c2f224a868ac541450c572 and manufactured by OSCOR INC.. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
a781428fe0c2f224a868ac541450c572
Registration Details
Taiwan FDA Registration: a781428fe0c2f224a868ac541450c572
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“BIOTRONIK”Senovo Bi-Flex Steerable Guiding Sheath
TW: “百多力”賽諾芙雙向可調控導引鞘
Risk Class 2
MD

Registration Details

a781428fe0c2f224a868ac541450c572

Ministry of Health Medical Device Import No. 036307

DHA05603630701

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E1340 Catheter Guide

Imported from abroad

Dates and Status

Feb 03, 2023

Feb 03, 2028