Taiwan FDA registration 888055a99ce6fe56f2e190a4bb4eeadf
"Serosi" Jacolay Q-switch Alexander laser
TW: “色若修”雅可蕾 Q-開關亞歷山大雷射
Taiwan·Risk Class 2·CYNOSURE, LLC·Registered Aug 19, 2008 – Aug 19, 2028ActiveRegistration details
- Analysis ID
- 888055a99ce6fe56f2e190a4bb4eeadf
- Customs Code
- DHA00601916708
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, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Aug 19, 2008
- Expiry Date
- Aug 19, 2028
About this record
Access comprehensive regulatory information for "Serosi" Jacolay Q-switch Alexander laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 888055a99ce6fe56f2e190a4bb4eeadf 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