Taiwan FDA registration 9402fb8c8902df16e295564d015e0534
“SCITON” mJoule System
TW: “西頓”迷你吉爾寬頻光照及雷射系統
Taiwan·Risk Class 2·MD·SCITON, INC.·Registered Aug 03, 2022 – Aug 03, 2027ActiveRegistration details
- Analysis ID
- 9402fb8c8902df16e295564d015e0534
- License Form
- Ministry of Health Medical Device Import No. 035731
- Customs Code
- DHA05603573109
Company information
- Manufacturer
- SCITON, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WOH MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 03, 2022
- Expiry Date
- Aug 03, 2027
About this record
Access comprehensive regulatory information for “SCITON” mJoule System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9402fb8c8902df16e295564d015e0534 and manufactured by SCITON, INC.. The authorized representative in Taiwan is WOH MEDICAL CO., LTD..
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