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“ClearStream” ReeFlex PTA Catheter - Taiwan Registration 34e0739db191a5e4f0fb1e6d1f41a5f4

Access comprehensive regulatory information for “ClearStream” ReeFlex 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 34e0739db191a5e4f0fb1e6d1f41a5f4 and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..

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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34e0739db191a5e4f0fb1e6d1f41a5f4
Registration Details
Taiwan FDA Registration: 34e0739db191a5e4f0fb1e6d1f41a5f4
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Device Details

“ClearStream” ReeFlex PTA Catheter
TW: “清流”銳弗斯經皮穿刺血管成形術導管
Risk Class 2
MD
Cancelled

Registration Details

34e0739db191a5e4f0fb1e6d1f41a5f4

Ministry of Health Medical Device Import No. 025814

DHA05602581407

Company Information

Product Details

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Feb 17, 2014

Feb 17, 2019

May 19, 2022

Cancellation Information

Logged out

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