Taiwan FDA registration b4323397ea3e4dd0daf23abe871eea08
“Syneron” elos Plus System
TW: “新那隆”伊樂思系統
Taiwan·Risk Class 2·MD·SYNERON MEDICAL LTD.·Registered Jul 08, 2014 – Jul 08, 2024ExpiredRegistration details
- Analysis ID
- b4323397ea3e4dd0daf23abe871eea08
- License Form
- Ministry of Health Medical Device Import No. 026331
- Customs Code
- DHA05602633105
Company information
- Manufacturer
- SYNERON MEDICAL LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- AESOLUTION BIOMEDICAL CO. 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 08, 2014
- Expiry Date
- Jul 08, 2024
About this record
Access comprehensive regulatory information for “Syneron” elos Plus System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b4323397ea3e4dd0daf23abe871eea08 and manufactured by SYNERON MEDICAL LTD.. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL CO. LTD..
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