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“Boston Scientific” AngioJet Ultra Power Pulse Kit - Taiwan Registration 4fc1da5feefdd7b707cf05d6049580e8

Access comprehensive regulatory information for “Boston Scientific” AngioJet Ultra Power Pulse Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4fc1da5feefdd7b707cf05d6049580e8 and manufactured by BOSTON SCIENTIFIC CORPORATION. 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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4fc1da5feefdd7b707cf05d6049580e8
Registration Details
Taiwan FDA Registration: 4fc1da5feefdd7b707cf05d6049580e8
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Device Details

“Boston Scientific” AngioJet Ultra Power Pulse Kit
TW: “波士頓科技”安傑特液體脈衝注射組
Risk Class 2
MD

Registration Details

4fc1da5feefdd7b707cf05d6049580e8

Ministry of Health Medical Device Import No. 028870

DHA05602887006

Company Information

Product Details

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

E Cardiovascular devices

E1210 Continuous Irrigation Catheter

Imported from abroad

Dates and Status

Oct 19, 2016

Oct 19, 2026