Taiwan FDA registration b86d9f7a1b6f431a355915ad6f6f07ea
"Asquebien" Kudrow Laser
TW: "阿斯克比恩" 庫卓雷射儀
Taiwan·Risk Class 2·ASCLEPION LASER TECHNOLOGIES GMBH·Registered Sep 21, 2005 – Sep 21, 2020CancelledRegistration details
- Analysis ID
- b86d9f7a1b6f431a355915ad6f6f07ea
- Customs Code
- DHA00601202801
Company information
- Manufacturer
- ASCLEPION LASER TECHNOLOGIES GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- COLLAMATRIX 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
- Sep 21, 2005
- Expiry Date
- Sep 21, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Asquebien" Kudrow Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b86d9f7a1b6f431a355915ad6f6f07ea and manufactured by ASCLEPION LASER TECHNOLOGIES GMBH. The authorized representative in Taiwan is COLLAMATRIX CO., LTD..
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