Taiwan FDA registration d6ee50aeb892aa6c3bb396cf3472365f
"Kanghe" multi-channel laser treatment instrument
TW: "康禾"多頻道雷射治療儀
Taiwan·Risk Class 2·KONFTEC CORPORATION·Registered Dec 15, 2006 – Dec 15, 2026ActiveRegistration details
- Analysis ID
- d6ee50aeb892aa6c3bb396cf3472365f
- Customs Code
- DHY00500210404
Company information
- Manufacturer
- KONFTEC CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- KONFTEC 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
- Domestic
Dates and status
- Registration Date
- Dec 15, 2006
- Expiry Date
- Dec 15, 2026
About this record
Access comprehensive regulatory information for "Kanghe" multi-channel laser treatment instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d6ee50aeb892aa6c3bb396cf3472365f and manufactured by KONFTEC CORPORATION. The authorized representative in Taiwan is KONFTEC CORPORATION.
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