Taiwan FDA registration 0031745a979aa2fc5191e4f50ab28b84
"Asquebien" Mideostar laser
TW: "阿斯克比恩" 密迪歐星雷射儀
Taiwan·Risk Class 2·ASCLEPION LASER TECHNOLOGIES GMBH·Registered Sep 26, 2005 – Sep 26, 2020CancelledRegistration details
- Analysis ID
- 0031745a979aa2fc5191e4f50ab28b84
- Customs Code
- DHA00601205705
Company information
- Manufacturer
- ASCLEPION LASER TECHNOLOGIES GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- Hair removal.
- 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
- Sep 26, 2005
- Expiry Date
- Sep 26, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Asquebien" Mideostar laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0031745a979aa2fc5191e4f50ab28b84 and manufactured by ASCLEPION LASER TECHNOLOGIES GMBH. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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