Taiwan FDA registration 85d676c93ceb2c9b6430805cd09fa9ed
"Mandro" diode laser system
TW: “蔓德蘿”二極體雷射系統
Taiwan·Risk Class 2·MEDRO MEDICAL DIVISION CO., LTD.·Registered Mar 20, 2012 – Mar 20, 2017CancelledRegistration details
- Analysis ID
- 85d676c93ceb2c9b6430805cd09fa9ed
- Customs Code
- DHA00602338201
Company information
- Manufacturer
- MEDRO MEDICAL DIVISION 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
- import
Dates and status
- Registration Date
- Mar 20, 2012
- Expiry Date
- Mar 20, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Mandro" 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 85d676c93ceb2c9b6430805cd09fa9ed and manufactured by MEDRO MEDICAL DIVISION CO., LTD.. The authorized representative in Taiwan is MAVIS MEDICAL ENTERPRISE CO., LTD..
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