Taiwan FDA registration 7d1e27336f00e7fd04bc0fe025a60a31
"Aurori" breast special MRI imaging system
TW: “奧羅瑞”乳房專用核磁共振影像系統
Taiwan·Risk Class 2·AURORA IMAGING TECHNOLOGY, INC.·Registered Apr 17, 2012 – Jun 06, 2017CancelledRegistration details
- Analysis ID
- 7d1e27336f00e7fd04bc0fe025a60a31
- Customs Code
- DHA00601811602
Company information
- Manufacturer
- AURORA IMAGING TECHNOLOGY, INC.
- Manufacturer Country
- United States
- Authorized Representative
- EDA TECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- P Radiology Science
- Import Information
- import
Dates and status
- Registration Date
- Apr 17, 2012
- Expiry Date
- Jun 06, 2017
- Cancellation Date
- Feb 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Aurori" breast special MRI 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 7d1e27336f00e7fd04bc0fe025a60a31 and manufactured by AURORA IMAGING TECHNOLOGY, INC.. The authorized representative in Taiwan is EDA TECHNOLOGY CO., LTD..
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