Wearable ECG biosensor
A lightweight, single-use chest patch continuously records two-channel ECG and patient-marked events for an extended monitoring period.
UltraLinQ Holter service
A complete Holter service, without building it alone.
An all-inclusive Holter pathway combining a lightweight ECG patch, secure cloud reporting and technician-reviewed preliminary reports ready for clinical interpretation.
Up to seven-day wear Secure cloud access Scalable provider workflow
Holter reporting workspace
Illustrative clinical workflow
De-identified study
Extended ECG recording
2 channelsEvent data
CH 1ECG waveform
CH 2ECG waveform
Data
Recovered
Analysis
Reviewed
Report
Awaiting sign-off
Wearable biosensor
Continuous ECG recording
One connected service
Device, data and reporting in one pathway.
Jace connects the patient-wear experience with the operational support needed to return a usable preliminary report to the clinical team.
Secure cloud workflow
Recorded data is uploaded into a controlled online environment for review, reporting and authorised access.
Technician-reviewed report
A cardiac technician reviews the recording and prepares a preliminary report ready for the responsible clinician’s interpretation.
The patient experience
Longer monitoring with less equipment to carry.
The LifeSignals 1AXe is a single-use, chest-worn Holter biosensor. Its wire-free design records ECG during daily life without a separate recorder box or loose leads.
Patients still need clear fitting, event-recording, water-exposure and return instructions. The technology simplifies the experience; it does not remove the need for a well-managed clinical pathway.
View the 1AXe biosensorTwo-channel ECG
Continuous ECG recording with heart-rate and patient-activated event information.
Up to seven days
Extended wear can increase the opportunity to capture intermittent symptoms and rhythm events.
Lightweight and wire-free
The 28g chest-worn patch avoids a separate recorder box and trailing lead wires.
Designed around daily life
Patients can sleep, move and follow the supplied water-resistance guidance while recording continues.
Wear duration, specifications and available workflow options can vary by market, regulatory clearance and service configuration.
End-to-end workflow
From patient enrolment to clinical interpretation.
A defined handoff at every stage helps keep the service safe, traceable and easier to scale.
01
Enrol and fit
The patient is enrolled in the agreed workflow and the single-use biosensor is applied to the upper chest.
02
Record normal life
ECG and event data are collected continuously while the patient follows the wear and symptom-diary instructions.
03
Recover the data
After monitoring, the biosensor data is securely transferred through the configured clinic or patient workflow.
04
Review and interpret
A technician-reviewed preliminary report is made available for clinician review, interpretation and sign-off.
Designed for clinical teams
A report supports the decision. It does not make it.
Technician review and ECG analysis can reduce the manual burden of preparing a Holter study, but the report remains preliminary until an appropriately qualified clinician interprets and signs it in context.
- Full-disclosure ECG waveforms available for authorised review
- Commenting, e-signature and audit-trail capability within the reporting workflow
- Clinical responsibility and escalation routes agreed during onboarding
Clinical reporting workflow
Controlled access and clear responsibility
Technician review
Preliminary findings and quality checks
Waveform access
Review the underlying ECG recording
Clinical comment
Add interpretation and follow-up
Authorisation
Sign-off with a traceable audit trail
Operational comparison
A different way to deliver ambulatory ECG.
Exact conventional Holter arrangements vary. This comparison focuses on the practical differences created by a single-use wireless patch and cloud reporting pathway.
ConsiderationConventional setupJace patch pathway
Patient equipmentRecorder and lead wiresSingle chest-worn patch
Wear periodDepends on service and deviceUp to seven days where configured
Daily routineMore equipment to manageWire-free with supplied care guidance
ReportingLocal workflow variesCloud access and technician review
Built to scale
For one consultant or a wider clinical service.
The workflow can be shaped around different enrolment volumes, reporting responsibilities and access requirements.
Independent consultants
Add extended Holter capability without building an entire analysis and reporting operation internally.
Private clinics
Offer a consistent monitoring pathway with cloud access and an operational workflow that can grow with demand.
Hospitals and cardiology units
Support higher-volume ambulatory ECG pathways with structured reporting and authorised team access.
Community services
Build an enrolment model around patients who need monitoring beyond a conventional hospital department.
Service questions
Before you introduce the pathway.
Practical questions about device wear, clinical responsibility, data access and provider scale.
Onboarding defines the service
Volumes, turnaround, governance and clinical ownership should be agreed before launch.
The service is designed to combine a single-use wearable ECG biosensor, the configured data-upload and cloud workflow, and a technician-reviewed preliminary Holter report. Exact onboarding, device supply, turnaround and clinical responsibilities should be agreed with Jace for your organisation.
Provider enquiries
Build the Holter service your team needs.
Tell Jace about your current pathway, expected volume and reporting requirements. The team can explain the available configuration and next steps.
UltraLinQ supports planned ambulatory cardiac investigation and reporting. It is not an emergency monitoring service. Patients with severe or rapidly worsening symptoms should follow urgent or emergency-care guidance.