Taiwan FDA registration 39ff093f8ed299619d61ad9cca90a687
Software for "Invivo" magnetic resonance diagnostic device
TW: “英維沃”磁振診斷裝置用軟體
Taiwan·Risk Class 2·INVIVO CORPORATION INC.·Registered May 07, 2007 – May 07, 2012CancelledRegistration details
- Analysis ID
- 39ff093f8ed299619d61ad9cca90a687
- Customs Code
- DHA00601805607
Company information
- Manufacturer
- INVIVO CORPORATION INC.
- Manufacturer Country
- United States
- Authorized Representative
- Bowex GmbH
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
- May 07, 2007
- Expiry Date
- May 07, 2012
- Cancellation Date
- May 05, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Software for "Invivo" magnetic resonance diagnostic device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 39ff093f8ed299619d61ad9cca90a687 and manufactured by INVIVO CORPORATION INC.. The authorized representative in Taiwan is Bowex GmbH.
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