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“Cordis” Sleek OTW Percutaneous Transluminal Angioplasty (PTA) Catheter - Taiwan Registration e2287868ee1135456282e369da1d98f3

Access comprehensive regulatory information for “Cordis” Sleek OTW Percutaneous Transluminal Angioplasty (PTA) Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e2287868ee1135456282e369da1d98f3 and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is EMERGO 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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e2287868ee1135456282e369da1d98f3
Registration Details
Taiwan FDA Registration: e2287868ee1135456282e369da1d98f3
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Device Details

“Cordis” Sleek OTW Percutaneous Transluminal Angioplasty (PTA) Catheter
TW: “考迪斯”速立刻擴張導管
Risk Class 2
MD

Registration Details

e2287868ee1135456282e369da1d98f3

Ministry of Health Medical Device Import No. 026374

DHA05602637400

Company Information

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 26, 2014

Jun 26, 2024