Taiwan FDA registration dcfb5b247a04a9a251862f837709ec84
“Coloplast” Conveen Critic Barrier (Non-sterile)
TW: “康樂保” 康維爾皮膚隔離霜 (未滅菌)
Taiwan·Risk Class 1·MD·COLOPLAST A/S·Registered Jul 15, 2014 – Jul 15, 2019CancelledRegistration details
- Analysis ID
- dcfb5b247a04a9a251862f837709ec84
- License Form
- Ministry of Health Medical Device Import No. 014327
- Customs Code
- DHA09401432705
Company information
- Manufacturer
- COLOPLAST A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- Taiwan Office of Hong Kong Commercial Coloplast Limited
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5090 Liquid bandages
- Import Information
- Imported from abroad; This permit was revoked by the Ministry of Health and Welfare Letter No. 1050006647 of 5/11/105 and is effective as of 15/11/105.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
- Registration Date
- Jul 15, 2014
- Expiry Date
- Jul 15, 2019
- Cancellation Date
- Nov 15, 2016
Cancellation information
- Status
- Logged out
About this record
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.
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