Taiwan FDA registration 94dfb8fa2a100f28552e2e0b6fcbb071

“Boston Scientific” Stingray LP Catheter

TW: “波士頓科技”史汀格導管

Taiwan·Risk Class 2·MD·BOSTON SCIENTIFIC CORPORATION·Registered Jun 03, 2016 – Jun 03, 2026Expired

Registration details

Analysis ID: 94dfb8fa2a100f28552e2e0b6fcbb071
License Form: Ministry of Health Medical Device Import No. 028601
Customs Code: DHA05602860105

Company information

Manufacturer: BOSTON SCIENTIFIC CORPORATION
Manufacturer Country: United States
Authorized Representative: Dutch Boston Technology Co., Ltd. Taiwan Branch

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): E Cardiovascular devices
Product Type (Level 2): E1250 Percutaneous catheter
Import Information: Imported from abroad

Dates and status

Registration Date: Jun 03, 2016
Expiry Date: Jun 03, 2026

About this record

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.