Pure Global

“Cordis” Savvy long Percutaneous Transluminal Angioplasty (PTA) Catheter - Taiwan Registration b06105f912da6d17ced168b8268471db

Access comprehensive regulatory information for “Cordis” Savvy long 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 b06105f912da6d17ced168b8268471db 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
b06105f912da6d17ced168b8268471db
Registration Details
Taiwan FDA Registration: b06105f912da6d17ced168b8268471db
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Cordis” Savvy long Percutaneous Transluminal Angioplasty (PTA) Catheter
TW: “考迪斯” 沙維長型PTA擴張導管
Risk Class 2
MD

Registration Details

b06105f912da6d17ced168b8268471db

Ministry of Health Medical Device Import No. 025250

DHA05602525000

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

Sep 30, 2013

Sep 30, 2023