Taiwan FDA registration 0323bfbe5017d0229e0b4c2f6f90aea7
"Benoy" non-motilated, single-patient, portable aspiration device (unsterilized)
TW: "貝諾"非動力式，單一病人使用，可攜帶式之抽吸器具(未滅菌)
Taiwan·Risk Class 1·BEINUOSI MEDICAL·Registered Mar 28, 2013 – Mar 28, 2018CancelledRegistration details
- Analysis ID
- 0323bfbe5017d0229e0b4c2f6f90aea7
- Customs Code
- DHA04600186601
Company information
- Manufacturer
- BEINUOSI MEDICAL
- Manufacturer Country
- China
- Authorized Representative
- ASIACONNECT INTERNATIONAL COMPANY LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of "non-powered, single-patient, portable suction device (I.4680)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4680 Non-motive, single patient-use, carry-on suctioning device
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Mar 28, 2013
- Expiry Date
- Mar 28, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Benoy" non-motilated, single-patient, portable aspiration device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0323bfbe5017d0229e0b4c2f6f90aea7 and manufactured by BEINUOSI MEDICAL. The authorized representative in Taiwan is ASIACONNECT INTERNATIONAL COMPANY LTD..
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