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Excimer laser angioplasty system - Taiwan Registration 482bed962f5b753f8fa1b4b8387c07a4

Access comprehensive regulatory information for Excimer laser angioplasty system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 482bed962f5b753f8fa1b4b8387c07a4 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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482bed962f5b753f8fa1b4b8387c07a4
Registration Details
Taiwan FDA Registration: 482bed962f5b753f8fa1b4b8387c07a4
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Device Details

Excimer laser angioplasty system
TW: ๆบ–ๅˆ†ๅญ้›ทๅฐ„่ก€็ฎกๆˆๅฝข่ก“็ณป็ตฑ
Risk Class 2

Registration Details

482bed962f5b753f8fa1b4b8387c07a4

DHA00600906405

Company Information

United States

Product Details

0699 Other Intensive Care Unit & Cardiac Care Unit Equipment

import

Dates and Status

Mar 22, 1999

Feb 09, 2029