Taiwan FDA registration 8a95d72402277f058420e9b5d842ba77
"Coloplast" Kangshuning Hernia Support Pair (Unsterilized)
TW: “康樂保”康束寧疝脫支撐束褲 (未滅菌)
Taiwan·Risk Class 1·COLOPLAST A/S·Registered Jun 22, 2007 – Jun 22, 2012CancelledRegistration details
- Analysis ID
- 8a95d72402277f058420e9b5d842ba77
- Customs Code
- DHA04400595909
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 recognition range of the hernia brace (H.5970) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5970 Hernia Removal Supporter
- Import Information
- import
Dates and status
- Registration Date
- Jun 22, 2007
- Expiry Date
- Jun 22, 2012
- Cancellation Date
- Apr 15, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Coloplast" Kangshuning Hernia Support Pair (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8a95d72402277f058420e9b5d842ba77 and manufactured by COLOPLAST A/S. The authorized representative in Taiwan is Taiwan Office of Hong Kong Commercial Coloplast Limited.
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