Taiwan FDA registration 84d6e830e41ad123d6dd38523ca0712d
"Daewoo" Enoma diode laser
TW: “大宇”愛諾瑪二極體雷射儀
Taiwan·Risk Class 2·DAEJU MEDITECH ENGINEERING·Registered Jul 03, 2018 – Jul 03, 2023ExpiredRegistration details
- Analysis ID
- 84d6e830e41ad123d6dd38523ca0712d
- Customs Code
- DHA05603127502
Company information
- Manufacturer
- DAEJU MEDITECH ENGINEERING
- 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
- Jul 03, 2018
- Expiry Date
- Jul 03, 2023
About this record
Access comprehensive regulatory information for "Daewoo" Enoma diode laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 84d6e830e41ad123d6dd38523ca0712d and manufactured by DAEJU MEDITECH ENGINEERING. The authorized representative in Taiwan is YUNGLIN BIOTECHNOLOGY CO., LTD..
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