Taiwan FDA registration 3ffeb237a5e230fe4bf97e3aa24f3099
“DEKA”SMARTXIDE LASER SYSTEM
TW: “德卡”絲瑪賽德雷射系統
Taiwan·Risk Class 2·MD·DEKA M.E.L.A. S.R.L.·Registered Jan 20, 2017 – Jan 20, 2027ActiveRegistration details
- Analysis ID
- 3ffeb237a5e230fe4bf97e3aa24f3099
- License Form
- Ministry of Health Medical Device Import No. 029351
- Customs Code
- DHA05602935100
Company information
- Manufacturer
- DEKA M.E.L.A. S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- NEOASIA LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 20, 2017
- Expiry Date
- Jan 20, 2027
About this record
Access comprehensive regulatory information for “DEKA”SMARTXIDE LASER SYSTEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3ffeb237a5e230fe4bf97e3aa24f3099 and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is NEOASIA LTD..
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