Taiwan FDA registration a32333e8891101368c1331aace845463

"Terumo" arterial filter

TW: "泰爾茂"動脈過濾器
Taiwan flagTaiwan·Risk Class 2·ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Jul 22, 1997 – Feb 09, 2029Active
Registration details
Analysis ID
a32333e8891101368c1331aace845463
Customs Code
DHA00600833709
Company information
Manufacturer Country
Japan
Authorized Representative
TERUMO TAIWAN MEDICAL CO., LTD.
Product details
Intended Use
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.4260 Cardiopulmonary vascular bypass artery blood spiller
Import Information
import
Dates and status
Registration Date
Jul 22, 1997
Expiry Date
Feb 09, 2029
About this record

Access comprehensive regulatory information for "Terumo" arterial filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a32333e8891101368c1331aace845463 and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

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