Taiwan FDA registration ce292de025b4aa803ea1ac6a8bcca82b
"Yoko" Nain Neodymium chromium laser
TW: “優科”娜茵釹雅鉻雷射儀
Taiwan·Risk Class 2·UTECH·Registered Feb 06, 2010 – Feb 06, 2015CancelledRegistration details
- Analysis ID
- ce292de025b4aa803ea1ac6a8bcca82b
- Customs Code
- DHA00602058704
Company information
- Manufacturer
- UTECH
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- UGINTECH CORPORATION
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
- Feb 06, 2010
- Expiry Date
- Feb 06, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Yoko" Nain Neodymium chromium laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce292de025b4aa803ea1ac6a8bcca82b and manufactured by UTECH. The authorized representative in Taiwan is UGINTECH CORPORATION.
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