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“Boston Scientific” Jetstream Jetwire Guidewire - Taiwan Registration 211e38119405b10ea86bc320e103c922

Access comprehensive regulatory information for “Boston Scientific” Jetstream Jetwire Guidewire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 211e38119405b10ea86bc320e103c922 and manufactured by Lake Region Medical. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.

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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211e38119405b10ea86bc320e103c922
Registration Details
Taiwan FDA Registration: 211e38119405b10ea86bc320e103c922
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Device Details

“Boston Scientific” Jetstream Jetwire Guidewire
TW: “波士頓科技”傑思楚導線
Risk Class 2
MD
Cancelled

Registration Details

211e38119405b10ea86bc320e103c922

Ministry of Health Medical Device Import No. 028892

DHA05602889203

Company Information

United States

Product Details

E Cardiovascular devices

E1330 Catheter Lead

Imported from abroad

Dates and Status

Nov 07, 2016

Nov 07, 2021

Aug 23, 2023

Cancellation Information

Logged out

許可證已逾有效期