Taiwan FDA registration 315efd4045e6a71a8f700634644fad6b
“DEKA” SMARTXIDE2 LASER SYSTEM
TW: “德卡”絲瑪雷射系統
Taiwan·Risk Class 2·MD·DEKA M.E.L.A. S.R.L.·Registered Jul 28, 2014 – Jul 28, 2024ExpiredRegistration details
- Analysis ID
- 315efd4045e6a71a8f700634644fad6b
- License Form
- Ministry of Health Medical Device Import No. 026356
- Customs Code
- DHA05602635608
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
- Jul 28, 2014
- Expiry Date
- Jul 28, 2024
About this record
Access comprehensive regulatory information for “DEKA” SMARTXIDE2 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 315efd4045e6a71a8f700634644fad6b and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is NEOASIA LTD..
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