Taiwan FDA registration 5fef9682fdd677f53e1ba18ee1ddd882

“Hexacath” PTCA Dilatation Catheter MISTRAL

TW: “海斯凱”敏追冠狀動脈氣球擴張導管
Taiwan flagTaiwan·Risk Class 3·MD·HEXACATH·Registered Feb 24, 2015 – Feb 24, 2025Expired
Registration details
Analysis ID
5fef9682fdd677f53e1ba18ee1ddd882
License Form
Ministry of Health Medical Device Import No. 027025
Customs Code
DHA05602702503
Company information
Manufacturer
HEXACATH
Manufacturer Country
France
Authorized Representative
CATHERINE CONSULTANTS CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular devices
Product Type (Level 2)
E0005 Percutaneous puncture of the coronary ductus
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 24, 2015
Expiry Date
Feb 24, 2025
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About this record

Access comprehensive regulatory information for “Hexacath” PTCA Dilatation Catheter MISTRAL in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5fef9682fdd677f53e1ba18ee1ddd882 and manufactured by HEXACATH. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HEXACATH, and 1 recent registrations in the same category. 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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