Taiwan FDA registration 9f47c058f22463b79c0adf7f1b585809

"Toray" Anssilon catheter

TW: "東麗" 安適龍導管
Taiwan flagTaiwan·Risk Class 2·TORAY INDUSTRIES, INC. SETA PLANT·Registered Sep 28, 1999 – Feb 09, 2029Active
Registration details
Analysis ID
9f47c058f22463b79c0adf7f1b585809
Customs Code
DHA00600931007
Company information
Manufacturer Country
Japan
Authorized Representative
HI-CLEARANCE INC.
Product details
Product Type (Level 1)
0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
Import Information
import
Dates and status
Registration Date
Sep 28, 1999
Expiry Date
Feb 09, 2029
About this record

Access comprehensive regulatory information for "Toray" Anssilon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9f47c058f22463b79c0adf7f1b585809 and manufactured by TORAY INDUSTRIES, INC. SETA PLANT. The authorized representative in Taiwan is HI-CLEARANCE 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