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"Termao" Tupperfer artificial blood vessels - Taiwan Registration 54a9bd14b6740bd86070c82fda3cce13

Access comprehensive regulatory information for "Termao" Tupperfer artificial blood vessels in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 54a9bd14b6740bd86070c82fda3cce13 and manufactured by VASCUTEK LTD.. 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.

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54a9bd14b6740bd86070c82fda3cce13
Registration Details
Taiwan FDA Registration: 54a9bd14b6740bd86070c82fda3cce13
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Device Details

"Termao" Tupperfer artificial blood vessels
TW: "ๆณฐ็ˆพ่Œ‚"็‰นๆ™ฎๅผ—ไบบๅทฅ่ก€็ฎก
Risk Class 2
Cancelled

Registration Details

54a9bd14b6740bd86070c82fda3cce13

DHA00601705207

Company Information

United Kingdom

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.3450 ่ก€็ฎก็งปๆคๅฝŒ่ฃœ็‰ฉ

import

Dates and Status

Aug 28, 2006

Aug 28, 2021

Oct 12, 2023

Cancellation Information

Logged out

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