Taiwan FDA registration b76960503c06a13edbb04728025113d5
"Mona" in vitro prosthesis (unsterilized)
TW: "夢娜"體外用義乳(未滅菌)
Taiwan·Risk Class 1·AMOENA MEDIZIN-ORTHOPÄDIE-TECHNIK GMBH·Registered Mar 09, 2011 – Mar 09, 2016CancelledRegistration details
- Analysis ID
- b76960503c06a13edbb04728025113d5
- Customs Code
- DHA04400999902
Company information
- Manufacturer
- AMOENA MEDIZIN-ORTHOPÄDIE-TECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- JE CHEENG INDUSTRAL CO., 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
- Mar 09, 2011
- Expiry Date
- Mar 09, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Mona" 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 b76960503c06a13edbb04728025113d5 and manufactured by AMOENA MEDIZIN-ORTHOPÄDIE-TECHNIK GMBH. The authorized representative in Taiwan is JE CHEENG INDUSTRAL CO., LTD..
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