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“Coloplast” Conveen Critic Barrier (Non-sterile) - Taiwan Registration dcfb5b247a04a9a251862f837709ec84

Access comprehensive regulatory information for “Coloplast” Conveen Critic Barrier (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dcfb5b247a04a9a251862f837709ec84 and manufactured by COLOPLAST A/S. The authorized representative in Taiwan is Taiwan Office of Hong Kong Commercial Coloplast Limited.

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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dcfb5b247a04a9a251862f837709ec84
Registration Details
Taiwan FDA Registration: dcfb5b247a04a9a251862f837709ec84
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Device Details

“Coloplast” Conveen Critic Barrier (Non-sterile)
TW: “康樂保” 康維爾皮膚隔離霜 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

dcfb5b247a04a9a251862f837709ec84

Ministry of Health Medical Device Import No. 014327

DHA09401432705

Company Information

Product Details

J General hospital and personal use equipment

J5090 Liquid bandages

Imported from abroad; This permit was revoked by the Ministry of Health and Welfare Letter No. 1050006647 of 5/11/105 and is effective as of 15/11/105.

Dates and Status

Jul 15, 2014

Jul 15, 2019

Nov 15, 2016

Cancellation Information

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