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Bayernik Haipang diagnostic catheter - Taiwan Registration da43c0dc0845b3afff9bc6e163d247dd

Access comprehensive regulatory information for Bayernik Haipang diagnostic catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number da43c0dc0845b3afff9bc6e163d247dd and manufactured by PENDRACARE INTERNATIONAL B.V.. The authorized representative in Taiwan is UNION-LINK CORPORATION.

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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da43c0dc0845b3afff9bc6e163d247dd
Registration Details
Taiwan FDA Registration: da43c0dc0845b3afff9bc6e163d247dd
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Device Details

Bayernik Haipang diagnostic catheter
TW: ๆ‹œ่€ณๅพทๅฐผๅ…‹ๆตทๆนƒ่จบๆ–ทๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

da43c0dc0845b3afff9bc6e163d247dd

DHA00602024502

Company Information

Netherlands

Product Details

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

E Cardiovascular Medicine Science

E.1200 ่จบๆ–ท็”จ่ก€็ฎกๅ…งๅฐŽ็ฎก

import

Dates and Status

Oct 16, 2009

Oct 16, 2014

Jun 26, 2018

Cancellation Information

Logged out

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