Taiwan FDA registration 6d734b996e7a585b70f887de8a2847f2
"Kanghe" portable laser therapy instrument
TW: “康禾”攜帶式雷射治療儀
Taiwan·Risk Class 2·KONFTEC CORPORATION·Registered Oct 30, 2008 – Oct 30, 2028ActiveRegistration details
- Analysis ID
- 6d734b996e7a585b70f887de8a2847f2
- Customs Code
- DHY00500254202
Company information
- Manufacturer
- KONFTEC CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- KONFTEC CORPORATION
Product details
- Intended Use
- Promotes wound healing. This product must be prescribed by a physician.
- 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
- Oct 30, 2008
- Expiry Date
- Oct 30, 2028
About this record
Access comprehensive regulatory information for "Kanghe" portable laser therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6d734b996e7a585b70f887de8a2847f2 and manufactured by KONFTEC CORPORATION. The authorized representative in Taiwan is KONFTEC CORPORATION.
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