Taiwan FDA registration 52aefa91880db672a11f6dfbbc8942a9
“OrthoScan” Mobile DI Mini C arm Imaging System
TW: “奧圖斯甘”行動數位迷你C臂X光機
Taiwan·Risk Class 2·MD·OrthoScan Inc.·Registered May 26, 2014 – May 26, 2019CancelledRegistration details
- Analysis ID
- 52aefa91880db672a11f6dfbbc8942a9
- License Form
- Ministry of Health Medical Device Import No. 026214
- Customs Code
- DHAS5602621409
Company information
- Manufacturer
- OrthoScan Inc.
- Manufacturer Country
- United States
- Authorized Representative
- WONDERLAND CORPORATION
Product details
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1650 fluoroscopic X-ray image intensifier
- Import Information
- Imported from abroad; Consent must be attached to the input (each input must be supported by the consent of the Atomic Energy Commission)
Dates and status
- Registration Date
- May 26, 2014
- Expiry Date
- May 26, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “OrthoScan” Mobile DI Mini C arm Imaging System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 52aefa91880db672a11f6dfbbc8942a9 and manufactured by OrthoScan Inc.. The authorized representative in Taiwan is WONDERLAND CORPORATION.
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