Taiwan FDA registration f891d463b86eb09a0d8b488e51c52e4e
"Byson" ruby laser system
TW: “拜森”紅寶石雷射系統
Taiwan·Risk Class 2·BISON MEDICAL CO., LTD·Registered Sep 26, 2016 – Sep 26, 2026ActiveRegistration details
- Analysis ID
- f891d463b86eb09a0d8b488e51c52e4e
- Customs Code
- DHA05602884609
Company information
- Manufacturer
- BISON MEDICAL CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MAVIS MEDICAL ENTERPRISE 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
- Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
Dates and status
- Registration Date
- Sep 26, 2016
- Expiry Date
- Sep 26, 2026
About this record
Access comprehensive regulatory information for "Byson" ruby 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 f891d463b86eb09a0d8b488e51c52e4e and manufactured by BISON MEDICAL CO., LTD. The authorized representative in Taiwan is MAVIS MEDICAL ENTERPRISE CO., LTD..
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