Taiwan FDA registration d63c5b868c42a1c95562859afd00bd80
"Metik" Mira Long Pulse Laser System
TW: “美提科”蜜拉長脈衝雷射系統
Taiwan·Risk Class 2·MEDIPARK·Registered Feb 12, 2018 – Feb 12, 2028ActiveRegistration details
- Analysis ID
- d63c5b868c42a1c95562859afd00bd80
- Customs Code
- DHA05603088001
Company information
- Manufacturer
- MEDIPARK
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- YUNGLIN BIOTECHNOLOGY 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
- Feb 12, 2018
- Expiry Date
- Feb 12, 2028
About this record
Access comprehensive regulatory information for "Metik" Mira Long Pulse 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 d63c5b868c42a1c95562859afd00bd80 and manufactured by MEDIPARK. The authorized representative in Taiwan is YUNGLIN BIOTECHNOLOGY CO., LTD..
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