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"Copenhagen" catheter fixation (unsterilized) - Taiwan Registration bce2526f3147cc3047bce16cfe2aa1d2

Access comprehensive regulatory information for "Copenhagen" catheter fixation (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bce2526f3147cc3047bce16cfe2aa1d2 and manufactured by COPENHAGEN MEDLAB. The authorized representative in Taiwan is Changyu Medical Equipment 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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bce2526f3147cc3047bce16cfe2aa1d2
Registration Details
Taiwan FDA Registration: bce2526f3147cc3047bce16cfe2aa1d2
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Device Details

"Copenhagen" catheter fixation (unsterilized)
TW: "ๅ“ฅๆœฌๅ“ˆๆ น" ๅฐŽ็ฎกๅ›บๅฎš่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

bce2526f3147cc3047bce16cfe2aa1d2

DHA04401079703

Company Information

Denmark

Product Details

Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the Measures for the Administration of Medical Devices.

J General hospital and personal use equipment

J.5210 ่ก€็ฎกๅ…งๅฐŽ็ฎกๅ›บๅฎš่ฃ็ฝฎ

import

Dates and Status

Sep 02, 2011

Sep 02, 2016

Apr 25, 2018

Cancellation Information

Logged out

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