Taiwan FDA registration a250750b577a0aec46031af467a9414f
“Syneron” eLase with Accessories
TW: “新納龍”伊蕾絲系統及配件
Registration details
- Analysis ID
- a250750b577a0aec46031af467a9414f
- License Form
- Ministry of Health Medical Device Import No. 027786
- Customs Code
- DHA05602778602
Company information
- Manufacturer
- SYNERON MEDICAL LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- Wo Medical Limited
Product details
- 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 17, 2015
- Expiry Date
- Sep 17, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Syneron” eLase 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 a250750b577a0aec46031af467a9414f and manufactured by SYNERON MEDICAL LTD.. The authorized representative in Taiwan is Wo Medical Limited.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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