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Learn about pioneering innovations; the use of diagnostics, data and AI in reproductive health; and the importance of policy and investment Join this event focused on the intersection of innovation,

High-risk elderly patients can successfully generate self-scanned lung ultrasound images comparable to those produced by physicians. These promising results warrant further investigation through larger-scale and long-term studies.

Perinatal care in obstetric care and Neonatology jam packed content will be in this year’s convention and we cant wait to learn more. Let’s meet there! https://worldperinatal.org/

The theme of the forthcoming Annual Congress is “Fueki Ryuko,” a philosophy advocated by Matsuo Basho, a renowned haiku poet of the 17th century, which means “immutability and fluidity” or

Biomed Israel 2025: The 23rd National Life Science & Technology Week • May 20-22, 2025 | David InterContinental • Tel Aviv, IsraelThis year’s conference is co-organized by leading Israeli and

Join us at the 2025 AIUM Annual Convention: The Ultrasound Event (formerly UltraCon), the world’s premier gathering of ultrasound clinicians, sonographers, radiologists, scientists, and industry. Gain insights from experts across

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FAQ

Frequently asked question

The Pulsenmore solution utilizes your smartphone’s processing and video streaming capabilities, communication protocols, display, and power resources. For this reason, not all smartphones meet the compatibility requirements. To insure your smartphone is compatible with the Pulsenmore Home Ultrasound check the Specification webpage.

Our commitment to patient safety and reliable scans guides the device’s design and functionality. The Pulsenmore device, connecting to a patient’s personal smartphone, optimally utilizes smartphone capabilities, minimizing material and resource consumption for enhanced environmental sustainability.

1. The Pulsenmore self-scan device is designed for use within a specific timeframe and usage limit. Extending its lifetime may compromise reading integrity due to material limitations.

2. Responsibility for device maintenance and home storage after the initial period cannot be assumed, impacting transducer quality and ultrasound scan reliability.

3. The device design and validated cleaning protocol do not allow transfer between patients, to avoid cross contamination and infection.

No, the product is subject to use in single pregnancies only.

The home ultrasound device is designed to provide continuity during pregnancy care and is intended to give you peace of mind.

Every scan requires medical interpretation, and it’s important to wait until the files are fully uploaded. You are not expected to understand or interpret the ultrasound scans; just follow the app’s instructions to scan, and receive a response from skilled ultrasound professionals .

You can view the scan in real-time while following the scanning instructions in the app. After the scan, the images are sent to the doctor and cannot be reviewed again.

In the App-Guided mode, the size of the zip file is about 20MB.The Clinician-Guided recorded scan is usually smaller, depending on the amount and length of clips.

Data is available for review for 30 days. During this time, the HCP can download and save the scans onto the patient file. More information is available in our Terms of Use.

No, the Clinician-Dashboard interface is an online web application that utilizes an active directory access technology (permission management tool).

The Pulsenmore Scan Key Code is generated by the HCP or admin within the clinician dashboard interface.It has unique identifiers based on the patient de-identified ID, selected mode (Clinician-Guided or App-Guided), and prescription details (frequency and time of use).The key is automatically transformed into a QR code and shared with the patient via email or SMS.

The device is designed for a single patient use, to prevent cross contamination.

Pulsenmore utilizes service logs and technical information to improve services and enhance user experience.Pseudonymized clinical data (also referred as de-identified data in the US) is used for clinical education,training, research and development purposes only.