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"Aridol" multi-channel infrared laser treatment instrument - Taiwan Registration 3220ee9cceaf4c7ca83a5036ac2f589d

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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3220ee9cceaf4c7ca83a5036ac2f589d
Registration Details
Taiwan FDA Registration: 3220ee9cceaf4c7ca83a5036ac2f589d
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Device Details

"Aridol" multi-channel infrared laser treatment instrument
TW: โ€œๆ„›้บ—ๆœต็ˆพโ€ๅคš้ ป้“็ด…ๅค–็ทš้›ทๅฐ„ๆฒป็™‚ๅ„€
Risk Class 2

Registration Details

3220ee9cceaf4c7ca83a5036ac2f589d

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

o Physical Medical Sciences;; I General, Plastic Surgery and Dermatology

O.5500 Infrared lamp;; I.4810 Lasers for general surgical, orthopaedic and dermatological use

Domestic

Dates and Status

Jun 07, 2017

Jun 07, 2027