Taiwan FDA registration a17c92a7f58773d448a77b224fc6eeca
"Serosi" Jacoland laser
TW: “色若修”雅可嵐雷射
Taiwan·Risk Class 2·CYNOSURE, INC.·Registered Nov 25, 2012 – Nov 25, 2017CancelledRegistration details
- Analysis ID
- a17c92a7f58773d448a77b224fc6eeca
- Customs Code
- DHA00602420102
Company information
- Manufacturer
- CYNOSURE, INC.
- Manufacturer Country
- United States
- Authorized Representative
- TBMS INTERNATIONAL 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
- Nov 25, 2012
- Expiry Date
- Nov 25, 2017
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Serosi" Jacoland laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a17c92a7f58773d448a77b224fc6eeca and manufactured by CYNOSURE, INC.. The authorized representative in Taiwan is TBMS INTERNATIONAL CORPORATION.
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