KardiaMobile Personal EKG (ECG) Device and Heart Monitor - Single-Lead EKG Recording - Detect AFib - FDA-Cleared - by AliveCor

£9.9
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KardiaMobile Personal EKG (ECG) Device and Heart Monitor - Single-Lead EKG Recording - Detect AFib - FDA-Cleared - by AliveCor

KardiaMobile Personal EKG (ECG) Device and Heart Monitor - Single-Lead EKG Recording - Detect AFib - FDA-Cleared - by AliveCor

RRP: £99
Price: £9.9
£9.9 FREE Shipping

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AFib), Bradycardia (a heart rate that’s too slow), Tachycardia (a condition that makes your heart beat more for using a Flexible Spending Account (FSA), Health Savings Account (HSA) or Health Reimbursement Account

KardiaMobile EKG Monitor Review - Healthline KardiaMobile EKG Monitor Review - Healthline

record your first EKG” on the homescreen of the mobile app. If it prompts you to allow the Kardia app toFor more articles like this direct to your inbox, sign up for our free monthly newsletter for healthcare professional

EKG Anywhere, Anytime | Kardia

Goldenthal IL, et al. (2019). Recurrent atrial fibrillation/flutter detection after ablation or cardioversion using the AliveCor KardiaMobile device: iHEART results. heartbeat that is the hallmark of atrial fibrillation. However, not all heart rate monitors and fitness Healthline has strict sourcing guidelines and relies on peer-reviewed studies, academic research institutions, and medical associations. We avoid using tertiary references. You can learn more about how we ensure our content is accurate and current by reading our editorial policy.

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The greater depth of detail from the KardiaMobile 6L provides doctors visibility into certain arrhythmias that are leading indicators of cardiovascular disease; this is not automatically indicated by the device, but can be read manually by the doctor from the rhythm strip. KardiaMobile 6L also features updated connectivity to your phone or tablet to prevent loss of connectivity due to interference from ultrasonic noise (eg. motion detectors, pest control devices, light switches). There are also minor cosmetic differences between devices. Clinicians went on to diagnose the cause of the symptoms in 69 out of 124 patients who were given the devices, compared to 11 of 116 in the control group.



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