Taiwan FDA registration 72ba29fb6cc5245e1ec6bae14afcd532
"Bolma" Imo segmented laser
TW: “寶樂瑪”伊莫分段式雷射儀
Taiwan·Risk Class 2·PALOMAR MEDICAL PRODUCTS INC.·Registered May 08, 2013 – May 08, 2018CancelledRegistration details
- Analysis ID
- 72ba29fb6cc5245e1ec6bae14afcd532
- Customs Code
- DHA00602500303
Company information
- Manufacturer
- PALOMAR MEDICAL PRODUCTS 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
- May 08, 2013
- Expiry Date
- May 08, 2018
- Cancellation Date
- Dec 09, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bolma" Imo segmented laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 72ba29fb6cc5245e1ec6bae14afcd532 and manufactured by PALOMAR MEDICAL PRODUCTS INC.. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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