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“Boston Scientific” Stingray LP Catheter - Taiwan Registration 94dfb8fa2a100f28552e2e0b6fcbb071

Access comprehensive regulatory information for “Boston Scientific” Stingray LP Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 94dfb8fa2a100f28552e2e0b6fcbb071 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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94dfb8fa2a100f28552e2e0b6fcbb071
Registration Details
Taiwan FDA Registration: 94dfb8fa2a100f28552e2e0b6fcbb071
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Device Details

“Boston Scientific” Stingray LP Catheter
TW: “波士頓科技”史汀格導管
Risk Class 2
MD

Registration Details

94dfb8fa2a100f28552e2e0b6fcbb071

Ministry of Health Medical Device Import No. 028601

DHA05602860105

Company Information

Product Details

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

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Jun 03, 2016

Jun 03, 2026