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"Coloplast" Kanghuier Wound Debridement Gel (Sterilized)  - Taiwan Registration 5540a681d17ab215c4f3c8264f3b242b

Access comprehensive regulatory information for "Coloplast" Kanghuier Wound Debridement Gel (Sterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5540a681d17ab215c4f3c8264f3b242b 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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5540a681d17ab215c4f3c8264f3b242b
Registration Details
Taiwan FDA Registration: 5540a681d17ab215c4f3c8264f3b242b
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Device Details

"Coloplast" Kanghuier Wound Debridement Gel (Sterilized) 
TW: "康樂保" 康惠爾傷口清創凝膠 (滅菌) 
Risk Class 1
Cancelled

Registration Details

5540a681d17ab215c4f3c8264f3b242b

DHA04400964009

Company Information

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".

I General, Plastic Surgery and Dermatology

I.4018 親水性創傷覆蓋材

QMS/QSD;; 輸入

Dates and Status

Dec 14, 2010

Dec 14, 2015

May 28, 2018

Cancellation Information

Logged out

許可證已逾有效期