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“DEKA”SMARTXIDE LASER SYSTEM - Taiwan Registration 3ffeb237a5e230fe4bf97e3aa24f3099

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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3ffeb237a5e230fe4bf97e3aa24f3099
Registration Details
Taiwan FDA Registration: 3ffeb237a5e230fe4bf97e3aa24f3099
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Device Details

“DEKA”SMARTXIDE LASER SYSTEM
TW: “德卡”絲瑪賽德雷射系統
Risk Class 2
MD

Registration Details

3ffeb237a5e230fe4bf97e3aa24f3099

Ministry of Health Medical Device Import No. 029351

DHA05602935100

Company Information

Italy

Product Details

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

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Jan 20, 2017

Jan 20, 2027