Taiwan FDA registration 467ba8dfbf85210f32c59422cd4247a6
"Becoen" in vitro cosmetic repair supplement (unsterilized)
TW: “必肯”體外美容用修復彌補物 (未滅菌)
Taiwan·Risk Class 1·BECON MEDICAL LIMITED·Registered May 12, 2011 – May 12, 2016CancelledRegistration details
- Analysis ID
- 467ba8dfbf85210f32c59422cd4247a6
- Customs Code
- DHA04401034902
Company information
- Manufacturer
- BECON MEDICAL LIMITED
- Manufacturer Country
- United States
- Authorized Representative
- Northwest Limited
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment management measures for in vitro cosmetic repair supplements (I.3800).
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3800 Repair supplement for cosmetic use in the body
- Import Information
- import
Dates and status
- Registration Date
- May 12, 2011
- Expiry Date
- May 12, 2016
- Cancellation Date
- Jun 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Becoen" in vitro cosmetic repair supplement (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 467ba8dfbf85210f32c59422cd4247a6 and manufactured by BECON MEDICAL LIMITED. The authorized representative in Taiwan is Northwest Limited.
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