Taiwan FDA registration e9f2f4285ce5915266c98d17d15b7503
"Quantel" diode laser system
TW: “寬特爾”二極體雷射系統
Taiwan·Risk Class 2·QUANTEL DERMA GMBH·Registered Aug 04, 2011 – Aug 04, 2016CancelledRegistration details
- Analysis ID
- e9f2f4285ce5915266c98d17d15b7503
- Customs Code
- DHA00602262509
Company information
- Manufacturer
- QUANTEL DERMA GMBH
- Manufacturer Country
- Germany
- 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
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Aug 04, 2011
- Expiry Date
- Aug 04, 2016
- Cancellation Date
- Feb 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 註銷藥商許可執照
About this record
Access comprehensive regulatory information for "Quantel" diode laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e9f2f4285ce5915266c98d17d15b7503 and manufactured by QUANTEL DERMA GMBH. The authorized representative in Taiwan is Dongzhe Riki Medical Co., Ltd.
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