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Breast Service Line*

Neuro

PATHOLOGY​

Breast Cancer​

VENDOR​

Transpara

APP Transpara​

DESCRIPTION​

Transpara® is a software device for automated detection of regions in mammograms suspicious for breast cancer.​​

MODALITY​​ 
X-Ray (2D & 3D)​

*Currently not available within the Calantic Viewer. Separately distributed by Bayer.​​

  1. ScreenPoint Transpara User Manual, software version 1.7.3

The clinical apps supplied on Calantic marketplace are from third parties and not manufactured or sponsored by Bayer or its affiliates. 

Bayer reserves the right to modify the specifications and features described herein or to discontinue any product or service identified in this publication at any time without prior notice or obligation. Please contact your authorised Bayer representative for the most current information.

© 2024 Bayer. This material may not be reproduced, displayed, modified or distributed without the express prior written consent of Bayer.

For Medical Information inquiries about Calantic, please contact medinfo.anz@bayer.com or 1800 008 757 (AU).

For medical inquiries relating to devices please contact your local Bayer representative.

 

Report Adverse Events

If you want to report an adverse event for medicines or devices, please contact your healthcare professional (e.g. physician or pharmacist) or the Therapeutic Goods Administration (TGA). Details on how to report to the TGA can be found at https://www.tga.gov.au/reporting-problems

Adverse events for devices should also be reported to Bayer via email to ricustomercomplaints@bayer.com

 

If you want to report a Quality Complaint

If you want to report a device quality complaint please contact ricustomercomplaints@bayer.com

 

Radiology

Bayer Australia Ltd

875 Pacific Highway, Pymble NSW 2073

ABN 22 000 138 714

 

© 2024 Bayer Pharmaceuticals

The clinical apps supplied on Calantic marketplace are from third parties and not manufactured or sponsored Bayer or its affiliates. 

Bayer reserves the right to modify the specifications and features described herein or to discontinue any product or service identified in this publication at any time without prior notice or obligation. Please contact your authorised Bayer representative for the most current information.

© 2024 Bayer. This material may not be reproduced,displayed, modified or distributed without the express prior written consent of Bayer.

For Medical Information relating to medicines please contact our Medical department at medinfo.anz@bayer.com or on 1800 008 757 (AU).

For medical inquiries relating to devices please contact your local Bayer representative.

 

Report Adverse Events

If you want to report an adverse event for medicines or devices, please contact your healthcare professional (e.g. physician or pharmacist) or the Therapeutic Goods Administration (TGA). Details on how to report to the TGA can be found at https://www.tga.gov.au/reporting-problems

Adverse events for medicines should also be reported to Bayer via email to drugsafety.anz@bayer.com or by phoning 1800 008 757.

Adverse events for devices should also be reported to Bayer via email to ricustomercomplaints@bayer.com

 

If you want to report a Quality Complaint

If you want to report a medicine quality complaint please contact drugsafety.anz@bayer.com

If you want to report a device quality complaint please contact ricustomercomplaints@bayer.com

 

Radiology

Bayer Australia Ltd

875 Pacific Highway, Pymble NSW 2073

ABN 22 000 138 714

 

PP-CALA-AU-0012-2

Date of preparation: July 2024

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