Taiwan FDA registration cdd2060ef4265867a74ddbf0163e374f
"Mandolin" in vitro prosthesis (unsterilized)
TW: "曼陀" 體外用義乳 (未滅菌)
Taiwan·Risk Class 1·MENTOR MEDICAL SYSTEMS B.V.·Registered May 24, 2011 – May 24, 2021CancelledRegistration details
- Analysis ID
- cdd2060ef4265867a74ddbf0163e374f
- Customs Code
- DHA04401039002
Company information
- Manufacturer
- MENTOR MEDICAL SYSTEMS B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
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 24, 2011
- Expiry Date
- May 24, 2021
- Cancellation Date
- May 31, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Mandolin" in vitro prosthesis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cdd2060ef4265867a74ddbf0163e374f and manufactured by MENTOR MEDICAL SYSTEMS B.V.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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