Taiwan FDA registration 2b62dca9aa2aa049ab4dbb9474160d0a
"Arthur" Guinenine infrared laser treatment device
TW: “亞瑟”健力適紅外線雷射治療儀
Taiwan·Risk Class 2·ASA s.r.l.·Registered Mar 14, 2020 – Mar 14, 2030ActiveRegistration details
- Analysis ID
- 2b62dca9aa2aa049ab4dbb9474160d0a
- Customs Code
- DHA05603339407
Company information
- Manufacturer
- ASA s.r.l.
- Manufacturer Country
- Italy
- Authorized Representative
- GAIA GENOMICS CORP.
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
- import
Dates and status
- Registration Date
- Mar 14, 2020
- Expiry Date
- Mar 14, 2030
About this record
Access comprehensive regulatory information for "Arthur" Guinenine infrared laser treatment device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b62dca9aa2aa049ab4dbb9474160d0a and manufactured by ASA s.r.l.. The authorized representative in Taiwan is GAIA GENOMICS CORP..
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