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"Toray" Anssilon catheter - Taiwan Registration 9f47c058f22463b79c0adf7f1b585809

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.

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9f47c058f22463b79c0adf7f1b585809
Registration Details
Taiwan FDA Registration: 9f47c058f22463b79c0adf7f1b585809
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Device Details

"Toray" Anssilon catheter
TW: "ๆฑ้บ—" ๅฎ‰้ฉ้พๅฐŽ็ฎก
Risk Class 2

Registration Details

9f47c058f22463b79c0adf7f1b585809

DHA00600931007

Company Information

Product Details

0699 Other Intensive Care Unit & Cardiac Care Unit Equipment

import

Dates and Status

Sep 28, 1999

Feb 09, 2029