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"Estellar" intravenous catheter - Taiwan Registration 85f54c197e16fe90166313c79f144f51

Access comprehensive regulatory information for "Estellar" intravenous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 85f54c197e16fe90166313c79f144f51 and manufactured by ENDOSCOPIC TECHNOLOGIES, INC.. The authorized representative in Taiwan is ASIA HEALTH CARE 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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85f54c197e16fe90166313c79f144f51
Registration Details
Taiwan FDA Registration: 85f54c197e16fe90166313c79f144f51
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Device Details

"Estellar" intravenous catheter
TW: โ€œ่‰พๆ–ฏๆณฐๆ ผโ€้œ่„ˆๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

85f54c197e16fe90166313c79f144f51

DHA00602051008

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing

import

Dates and Status

Dec 23, 2009

Dec 23, 2014

Jul 31, 2018

Cancellation Information

Logged out

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