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HI-TORQUE Proceed Guide Wire - Taiwan Registration 6577be9a0f29849059632ea00ca6a938

Access comprehensive regulatory information for HI-TORQUE Proceed 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 6577be9a0f29849059632ea00ca6a938 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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6577be9a0f29849059632ea00ca6a938
Registration Details
Taiwan FDA Registration: 6577be9a0f29849059632ea00ca6a938
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Device Details

HI-TORQUE Proceed Guide Wire
TW: ้ซ˜้ธๆ ผๆณข่ฅฟ่ก€็ฎกๅฐŽ็ทš
Risk Class 2
MD

Registration Details

6577be9a0f29849059632ea00ca6a938

Ministry of Health Medical Device Import No. 034549

DHA05603454902

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular devices

E1330 Catheter Lead

Imported from abroad

Dates and Status

Jun 09, 2021

Jun 09, 2026