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“BIOTRONIK” Passeo-35 HP PTA Balloon Dilatation Catheter - Taiwan Registration 829e0b2c623b4ed58914e3dc3696538c

Access comprehensive regulatory information for “BIOTRONIK” Passeo-35 HP PTA Balloon Dilatation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 829e0b2c623b4ed58914e3dc3696538c and manufactured by Creagh Medical Ltd.. 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.

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829e0b2c623b4ed58914e3dc3696538c
Registration Details
Taiwan FDA Registration: 829e0b2c623b4ed58914e3dc3696538c
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Device Details

“BIOTRONIK” Passeo-35 HP PTA Balloon Dilatation Catheter
TW: “百多力”帕希爾35高壓周邊血管周邊氣球擴張導管
Risk Class 2
MD

Registration Details

829e0b2c623b4ed58914e3dc3696538c

Ministry of Health Medical Device Import No. 029140

DHA05602914000

Company Information

Ireland

Product Details

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

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Dec 09, 2016

Dec 09, 2026