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Device Compatibility Review is available for enquiries. Monitoring technology is under development: no patient monitoring or device connections are active.

Monitoring pathways

Pathways under consideration.

Monitoring requirements depend on the patient's condition, treatment plan and clinical assessment. Each pathway would follow the treating hospital's prescribed plan; CrossCare does not set clinical monitoring requirements.

  • Diabetes and metabolic health

    Requirements set by the treating clinicians.

  • Cardiovascular recovery

    Requirements set by the treating clinicians.

  • Oncology follow-up

    Requirements set by the treating clinicians.

  • Stroke and neurological rehabilitation

    Requirements set by the treating clinicians.

  • Orthopedic and surgical recovery

    Requirements set by the treating clinicians.

  • Respiratory health and sleep apnea

    Requirements set by the treating clinicians.

  • Elderly and complex care

    Requirements set by the treating clinicians.

  • Other clinician-approved post-treatment pathways

    Requirements set by the treating clinicians.

These pathways describe areas being considered for the proposed service. They are not treatment programmes and do not imply that monitoring is currently available for any condition.

Any future monitoring would use approved medical devices where appropriate, alongside patient-reported information, and would be agreed between the treating hospital and appropriately licensed local professionals.

Device category

Weight & Body Composition Monitoring

Connected weight and body composition scales are now included in the device categories CrossCare can discuss through a Device Compatibility Review. Any monitoring use would be set by the treating clinicians.

  • Device categoryIncluded for compatibility enquiries
  • Transtek SFZ41Manufacturer integration not yet verified
  • Automated transmission to CrossCare or hospital dashboardsUnder Development

Potential monitoring applications

Possible future uses under consideration, not services offered today. Each would follow a plan set by licensed clinicians.

  • Weight management

    Tracking weight trends alongside a clinician-supervised weight management or metabolic programme.

  • Post-discharge follow-up

    Giving the treating team a view of weight changes they have asked to follow after the patient returns home.

  • Rehabilitation

    Supporting rehabilitation teams who track weight or body composition during recovery.

  • Elderly care

    Helping families and carers keep up regular weigh-ins that a clinician has requested.

  • Clinician-directed recovery programmes

    Forming one part of a recovery plan designed and reviewed by licensed clinicians.

Example device under evaluation

Transtek Body Fat Scale SFZ41

Manufacturer integration not yet verified

The manufacturer describes the SFZ41 as a body fat scale using bioelectrical impedance analysis (BIA) and lists a supported phone app on its product page. CrossCare has not tested or verified this.

Shown only as an example of a device CrossCare is evaluating. There is no Transtek partnership, API integration or clinical certification by CrossCare, and cross-border connectivity is not guaranteed. Listing this device is not an endorsement or recommendation.

Manufacturer product page (external site)

Device categories included for compatibility enquiries

  • Continuous glucose monitor (CGM)
  • Blood pressure monitor
  • ECG device
  • Pulse oximeter
  • Cardiac monitoring device
  • Sleep monitoring device
  • Weight & body composition scale
  • Other devices on request

Please do not enter body weight, body-fat percentages or any other measurements in the checker or enquiry forms. They are not needed and will be rejected.

Hospital partners

Interested in a hospital partnership?

Tell us about your international patient programme. Our team will follow up about pilot participation and the proposed service.

Become a Hospital Partner

Device Compatibility Review is an enquiry-based coordination service. CrossCare does not collect patient health data or provide live monitoring through these pages. Any future clinical capability will require separate design, security, privacy, regulatory and clinical governance review before launch. CrossCare coordinates care with licensed providers and does not diagnose or replace a doctor.

CrossCare Global Connected Recovery™ provides international care coordination and technology connectivity support. Clinical monitoring, diagnosis, treatment decisions and emergency responses remain the responsibility of appropriately licensed healthcare professionals. Device compatibility and monitoring availability depend on manufacturer authorization, technical validation and applicable regulatory requirements.

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