Taiwan FDA registration aa47c8c99cd12fb42b17213e856595f3
Philips magnetic resonance imaging software system
TW: 飛利浦磁振造影軟體系統
Taiwan·Risk Class 2·INVIVO CORPORATION·Registered Oct 18, 2010 – Oct 18, 2015CancelledRegistration details
- Analysis ID
- aa47c8c99cd12fb42b17213e856595f3
- Customs Code
- DHA00602158301
Company information
- Manufacturer
- INVIVO CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1000 磁振診斷裝置
- Import Information
- import
Dates and status
- Registration Date
- Oct 18, 2010
- Expiry Date
- Oct 18, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Philips magnetic resonance imaging software system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa47c8c99cd12fb42b17213e856595f3 and manufactured by INVIVO CORPORATION. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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