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“Abbott” HI-TORQUE JET Guide Wire - Taiwan Registration 6345ac346db1d7fd7ff3426613dd70fa

Access comprehensive regulatory information for “Abbott” HI-TORQUE JET 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 6345ac346db1d7fd7ff3426613dd70fa and manufactured by ABBOTT VASCULAR. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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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6345ac346db1d7fd7ff3426613dd70fa
Registration Details
Taiwan FDA Registration: 6345ac346db1d7fd7ff3426613dd70fa
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Device Details

“Abbott” HI-TORQUE JET Guide Wire
TW: “亞培”高鐸格捷特導線
Risk Class 2
MD

Registration Details

6345ac346db1d7fd7ff3426613dd70fa

Ministry of Health Medical Device Import No. 027222

DHA05602722205

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

Mar 13, 2015

Mar 13, 2025