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“BIOTRONIK” Passeo-14 Peripheral Dilatation Catheter - Taiwan Registration e45c2c8b55a0dff686ae38bda5e88395

Access comprehensive regulatory information for “BIOTRONIK” Passeo-14 Peripheral 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 e45c2c8b55a0dff686ae38bda5e88395 and manufactured by BIOTRONIK AG. 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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e45c2c8b55a0dff686ae38bda5e88395
Registration Details
Taiwan FDA Registration: e45c2c8b55a0dff686ae38bda5e88395
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Device Details

“BIOTRONIK” Passeo-14 Peripheral Dilatation Catheter
TW: “百多力”帕希爾14周邊氣球擴張導管
Risk Class 2
MD

Registration Details

e45c2c8b55a0dff686ae38bda5e88395

Ministry of Health Medical Device Import No. 027320

DHA05602732005

Company Information

Switzerland

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

Jun 09, 2015

Jun 09, 2025