Taiwan FDA registration a57cf002a4bb6c6e9be1fa6c11f2406e
"Mitoyo" medical image transmission device (unsterilized)
TW: “三豐”醫學影像傳輸裝置 (未滅菌)
Taiwan·Risk Class 1·BENQ MEDICAL TECHNOLOGY CORPORATION·Registered Aug 25, 2009 – Aug 25, 2014CancelledRegistration details
- Analysis ID
- a57cf002a4bb6c6e9be1fa6c11f2406e
Company information
- Manufacturer
- BENQ MEDICAL TECHNOLOGY CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first-level recognition range of medical image transmission devices (P.2020) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.2020 Medical imaging communication devices
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 25, 2009
- Expiry Date
- Aug 25, 2014
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Mitoyo" medical image transmission 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 a57cf002a4bb6c6e9be1fa6c11f2406e and manufactured by BENQ MEDICAL TECHNOLOGY CORPORATION. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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