Taiwan FDA registration 52cf95e58086a59f16a348efe46cc424
"Asquebian" Kudjoplas Laser
TW: “阿斯克比恩”庫卓普拉斯雷射儀
Taiwan·Risk Class 2·ASCLEPION LASER TECHNOLOGIES GMBH·Registered Sep 30, 2011 – Sep 30, 2016CancelledRegistration details
- Analysis ID
- 52cf95e58086a59f16a348efe46cc424
- Customs Code
- DHA00602287200
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
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Sep 30, 2011
- Expiry Date
- Sep 30, 2016
- Cancellation Date
- Jun 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Asquebian" Kudjoplas Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 52cf95e58086a59f16a348efe46cc424 and manufactured by ASCLEPION LASER TECHNOLOGIES GMBH. The authorized representative in Taiwan is COLLAMATRIX CO., LTD..
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