Taiwan FDA registration fbbf971a938e6faf03f5e1ca1ac29b79
"Denona" diode laser
TW: “黛諾娜”二極體雷射儀
Taiwan·Risk Class 2·DINONA INC.·Registered Apr 13, 2009 – Apr 13, 2014CancelledRegistration details
- Analysis ID
- fbbf971a938e6faf03f5e1ca1ac29b79
- Customs Code
- DHA00601977403
Company information
- Manufacturer
- DINONA INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Dongzhe Riki Medical Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Import Information
- import
Dates and status
- Registration Date
- Apr 13, 2009
- Expiry Date
- Apr 13, 2014
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Denona" diode laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fbbf971a938e6faf03f5e1ca1ac29b79 and manufactured by DINONA INC.. The authorized representative in Taiwan is Dongzhe Riki Medical Co., Ltd.
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