Taiwan FDA registration 1e17a621b0495de0e58ab006612d1131
"Bolema" pulsed light and laser system
TW: "寶樂瑪"脈衝光及雷射系統
Taiwan·Risk Class 2·PALOMAR MEDICAL TECHNOLOGIES, INC.·Registered Jul 12, 2006 – Jul 12, 2016CancelledRegistration details
- Analysis ID
- 1e17a621b0495de0e58ab006612d1131
- Customs Code
- DHA00601687201
Company information
- Manufacturer
- PALOMAR MEDICAL TECHNOLOGIES, INC.
- Manufacturer Country
- United States
- 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, 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
- Jul 12, 2006
- Expiry Date
- Jul 12, 2016
- Cancellation Date
- May 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bolema" pulsed light and laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1e17a621b0495de0e58ab006612d1131 and manufactured by PALOMAR MEDICAL TECHNOLOGIES, INC.. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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