Taiwan FDA registration 658c3ebe1460577e13bdc7f4ebaed528
“EFB” Intense Pulsed Light
TW: “伊膚寶”脈衝光治療儀
Taiwan·Risk Class 2·MD·EUROFEEDBACK SAS·Registered Nov 17, 2014 – Nov 17, 2019CancelledRegistration details
- Analysis ID
- 658c3ebe1460577e13bdc7f4ebaed528
- License Form
- Ministry of Health Medical Device Import No. 026785
- Customs Code
- DHA05602678505
Company information
- Manufacturer
- EUROFEEDBACK SAS
- Manufacturer Country
- France
- Authorized Representative
- CROWNMED ENTERPRISE CO., LTD.
Product details
- 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 17, 2014
- Expiry Date
- Nov 17, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “EFB” Intense Pulsed Light in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 658c3ebe1460577e13bdc7f4ebaed528 and manufactured by EUROFEEDBACK SAS. The authorized representative in Taiwan is CROWNMED ENTERPRISE CO., LTD..
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