Taiwan FDA registration 482bed962f5b753f8fa1b4b8387c07a4

Excimer laser angioplasty system

TW: 準分子雷射血管成形術系統
Taiwan flagTaiwan·Risk Class 2·SPECTRANETICS CORPORATION·Registered Mar 22, 1999 – Feb 09, 2029Active
Registration details
Analysis ID
482bed962f5b753f8fa1b4b8387c07a4
Customs Code
DHA00600906405
Company information
Manufacturer Country
United States
Authorized Representative
LORION ENTERPRISES INC.
Product details
Product Type (Level 1)
0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
Import Information
import
Dates and status
Registration Date
Mar 22, 1999
Expiry Date
Feb 09, 2029
About this record

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.

Free DatabasePowered by Pure Global AI89,000+ Devices