Taiwan FDA registration 5540a681d17ab215c4f3c8264f3b242b
"Coloplast" Kanghuier Wound Debridement Gel (Sterilized)
TW: "康樂保" 康惠爾傷口清創凝膠 (滅菌)
Taiwan·Risk Class 1·COLOPLAST A/S·Registered Dec 14, 2010 – Dec 14, 2015CancelledRegistration details
- Analysis ID
- 5540a681d17ab215c4f3c8264f3b242b
- Customs Code
- DHA04400964009
Company information
- Manufacturer
- COLOPLAST A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- Taiwan Office of Hong Kong Commercial Coloplast Limited
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4018 親水性創傷覆蓋材
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 14, 2010
- Expiry Date
- Dec 14, 2015
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
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.
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