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This User Guide is for the Portal of the B4C System. For guidance on setup and practical application of the actual sensor and/or mobile app components, please refer to the https://brain4care.atlassian.net/wiki/spaces/B4CSENSORGUIDE29B4CSENSORGUIDE30.

Please review the brain4care portal information carefully. This guide contains essential information for the correct usage of the B4C System. It is important to review it thoroughly. Should you have any inquiries, feel free to contact our technical support team for assistance.

The B4C System was developed following the most up to date information and security protocols and is compliant with General Data Protection Act (LGPD, Brazil) and the Health Insurance Portability and Accountability Act (HIPAA, USA). The architecture ensures internal de-identification of patient data while allowing healthcare professionals, who are licensed to use the wireless noninvasive intracranial pressure monitoring system, to view and analyze intracranial pressure morphology data. This secure architecture does NOT preclude the existence of some rules that must be fully followed by users for the correct use and operation of the platform:

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  • Always use nationally or internationally recognized scientific protocols for sensor use and data analysis on the portal.

  • The proper functioning of the platform depends on installing the Google Chrome, Microsoft Edge, or Firefox browser on your computer, laptop, or tablet. Appropriate internet connection is also required.

  • Read this user guide in its entirety, as many questions can be avoided by knowing system functions.

  • The images presented in this manual are for illustration purposes only.

  • Please refer to the https://brain4care.atlassian.net/wiki/spaces/B4CSENSORGUIDE29B4CSENSORGUIDE30 for more information regarding the interpretation of the report information.

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  • Undergone decompression craniectomy;

  • Cranial defects (missing skull portion);

  • Patients with hypersensitivity to sensor components;

  • Other conditions that the healthcare professional deems unsuitable for use of this device.

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