Taiwan FDA registration 3220ee9cceaf4c7ca83a5036ac2f589d
"Aridol" multi-channel infrared laser treatment instrument
TW: “愛麗朵爾”多頻道紅外線雷射治療儀
Taiwan·Risk Class 2·WELLMIKE TECHNOLOGY CORPORATION·Registered Jun 07, 2017 – Jun 07, 2027ActiveRegistration details
- Analysis ID
- 3220ee9cceaf4c7ca83a5036ac2f589d
Company information
- Manufacturer
- WELLMIKE TECHNOLOGY CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WELLMIKE TECHNOLOGY CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences;; I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- O.5500 Infrared lamp;; I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- Domestic
Dates and status
- Registration Date
- Jun 07, 2017
- Expiry Date
- Jun 07, 2027
About this record
Access comprehensive regulatory information for "Aridol" multi-channel infrared 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 3220ee9cceaf4c7ca83a5036ac2f589d and manufactured by WELLMIKE TECHNOLOGY CORPORATION. The authorized representative in Taiwan is WELLMIKE TECHNOLOGY CORPORATION.
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