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“Abbott” Hi-Torque Cross-IT XT Guide Wire - Taiwan Registration 41cfc97f3f707fccd5c9f2a63f3fadb6

Access comprehensive regulatory information for “Abbott” Hi-Torque Cross-IT XT Guide Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 41cfc97f3f707fccd5c9f2a63f3fadb6 and manufactured by ABBOTT VASCULAR. The authorized representative in Taiwan is Abbott Medical Taiwan Co..

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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41cfc97f3f707fccd5c9f2a63f3fadb6
Registration Details
Taiwan FDA Registration: 41cfc97f3f707fccd5c9f2a63f3fadb6
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Device Details

“Abbott” Hi-Torque Cross-IT XT Guide Wire
TW: “亞培”高鐸格擴司通導管引線
Risk Class 2
MD

Registration Details

41cfc97f3f707fccd5c9f2a63f3fadb6

Ministry of Health Medical Device Import No. 029258

DHA05602925800

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E1330 Catheter Lead

Imported from abroad

Dates and Status

Dec 26, 2016

Dec 26, 2026