ACTIMI Signals · Optional medical-device module
From eligible vital readings to alert decisions.
Add ACTIMI Signals to your digital health application through Ovok. Enroll patients individually, send eligible readings for evaluation and bring alert decisions into your care workflow.
Jonas BeckerOxygen saturation%Reviewed
Mia SchulzWeightkgNot enrolled
Lena HoffmannBlood pressuremmHgNo alertLena HoffmannBlood pressuremmHgReviewedMia SchulzOxygen saturation%Not enrolledJonas BeckerWeightkgNo alert- 01
Enroll the patient
Configure Signals per patient. Patients without Signals enrollment can still use the FHIR backend and supported-device data.
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Evaluate eligible readings
Only eligible vital-sign readings from enrolled patients are forwarded to Signals. Device ingestion and clinical evaluation are separate steps.
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Bring decisions into care
Use the returned alert decisions in your application. Your care team defines the review, escalation and response workflow.
A clear regulatory boundary
ACTIMI Signals is an MDR Class IIa medical device. Ovok’s FHIR backend is not itself a certified medical device, and using Signals does not automatically certify your application. Review intended use and integration requirements with ACTIMI.
Talk to ACTIMI →One platform. Patient-level choice.
Growth and Scale include Signals and one supported device per monitored patient. A monitored patient has at least one Signals evaluation in a calendar month. Compare plans and estimate your usage before moving to production.