Taiwan FDA registration 8d5ea1afc4689f2c7a7263c022520e2d
“Cynosure” Elite+ Laser
TW: “色若修”伊儷雷射
Taiwan·Risk Class 2·MD·CYNOSURE, LLC·Registered Nov 15, 2013 – Nov 15, 2023ExpiredRegistration details
- Analysis ID
- 8d5ea1afc4689f2c7a7263c022520e2d
- License Form
- Ministry of Health Medical Device Import No. 025599
- Customs Code
- DHA05602559903
Company information
- Manufacturer
- CYNOSURE, LLC
- Manufacturer Country
- United States
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
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
- Nov 15, 2013
- Expiry Date
- Nov 15, 2023
About this record
Access comprehensive regulatory information for “Cynosure” Elite+ Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8d5ea1afc4689f2c7a7263c022520e2d and manufactured by CYNOSURE, LLC. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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.
Free DatabasePowered by Pure Global AI89,000+ Devices