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“TMP” Rescue Balloon Occlusion Catheter - Taiwan Registration f0eb5ac0931451302795b668ef72c23f

Access comprehensive regulatory information for “TMP” Rescue Balloon Occlusion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0eb5ac0931451302795b668ef72c23f and manufactured by Tokai Medical Products, Inc., Toki Factory. The authorized representative in Taiwan is HI-CLEARANCE INC..

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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f0eb5ac0931451302795b668ef72c23f
Registration Details
Taiwan FDA Registration: f0eb5ac0931451302795b668ef72c23f
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Device Details

“TMP” Rescue Balloon Occlusion Catheter
TW: “東海”銳思克閉塞球囊導管
Risk Class 2
MD

Registration Details

f0eb5ac0931451302795b668ef72c23f

Ministry of Health Medical Device Import No. 032086

DHA05603208604

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

Jan 23, 2019

Jan 23, 2024