Pure Global

“Spectranetics” Quick-Cross Capture Guidewire Retriever - Taiwan Registration 68824d946b2265504b42d057bfe541e2

Access comprehensive regulatory information for “Spectranetics” Quick-Cross Capture Guidewire Retriever in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68824d946b2265504b42d057bfe541e2 and manufactured by SPECTRANETICS CORPORATION. The authorized representative in Taiwan is LORION ENTERPRISES INC..

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
68824d946b2265504b42d057bfe541e2
Registration Details
Taiwan FDA Registration: 68824d946b2265504b42d057bfe541e2
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Spectranetics” Quick-Cross Capture Guidewire Retriever
TW: “史特勞斯”區克斯開普斯導線回收器
Risk Class 2
MD
Cancelled

Registration Details

68824d946b2265504b42d057bfe541e2

Ministry of Health Medical Device Import No. 026452

DHA05602645204

Company Information

United States

Product Details

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Aug 28, 2014

Aug 28, 2019

Jul 15, 2022

Cancellation Information

Logged out

未展延而逾期者