Taiwan FDA registration b6c25f9a4382d9e587dc5467713d7e91

“Eurocor” DIOR Paclitaxel eluting PTCA balloon catheter

TW: “優洛可”笛沃心臟經皮冠狀動脈氣球擴張導管

Taiwan·Risk Class 3·MD·Eurocor Tech GmbH·Registered Aug 05, 2014 – Aug 05, 2024Expired

Registration details

Analysis ID: b6c25f9a4382d9e587dc5467713d7e91
License Form: Ministry of Health Medical Device Import No. 026423
Customs Code: DHA05602642300

Company information

Manufacturer: Eurocor Tech GmbH
Manufacturer Country: Germany
Authorized Representative: SUNNY HEART SCIENTIFIC 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: Aug 05, 2014
Expiry Date: Aug 05, 2024

About this record

Access comprehensive regulatory information for “Eurocor” DIOR Paclitaxel eluting PTCA balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number b6c25f9a4382d9e587dc5467713d7e91 and manufactured by Eurocor Tech GmbH. The authorized representative in Taiwan is SUNNY HEART SCIENTIFIC 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.