Taiwan FDA registration b765e56428ba52f3367b5a34ebcca563
“Syneron” VelaShape III System with Accessories
TW: “新納龍”薇拉三代非侵入性電波系統及配件
Taiwan·Risk Class 2·MD·SYNERON MEDICAL LTD.·Registered Sep 20, 2023 – Jan 27, 2026ExpiredRegistration details
- Analysis ID
- b765e56428ba52f3367b5a34ebcca563
- License Form
- Ministry of Health Medical Device Import No. 028176
- Customs Code
- DHA05602817603
Company information
- Manufacturer
- SYNERON MEDICAL LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- DYNAMIC MEDICAL TECHNOLOGIES INC.
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
- Sep 20, 2023
- Expiry Date
- Jan 27, 2026
About this record
Access comprehensive regulatory information for “Syneron” VelaShape III System with Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b765e56428ba52f3367b5a34ebcca563 and manufactured by SYNERON MEDICAL LTD.. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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