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“Spectranetics” Stellarex Drug-Coated Angioplasty Balloon - Taiwan Registration 2f3ae26febc4195d5c2d82cdd3748c7e

Access comprehensive regulatory information for “Spectranetics” Stellarex Drug-Coated Angioplasty Balloon in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f3ae26febc4195d5c2d82cdd3748c7e 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.

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2f3ae26febc4195d5c2d82cdd3748c7e
Registration Details
Taiwan FDA Registration: 2f3ae26febc4195d5c2d82cdd3748c7e
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Device Details

“Spectranetics” Stellarex Drug-Coated Angioplasty Balloon
TW: “史特勞斯”司特樂塗藥球囊導管
Risk Class 2
MD

Registration Details

2f3ae26febc4195d5c2d82cdd3748c7e

Ministry of Health Medical Device Import No. 033806

DHA05603380604

Company Information

United States

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

Jul 02, 2020

Jul 02, 2025