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Important to know:

The Pulsenmore ES ultrasound system is FDA-authorized for prescribed use to support limited prenatal ultrasound imaging for determination of fetal heart rate in singleton pregnancies between 14–38 weeks of gestation. Images are reviewed and interpreted by a physician.The device is authorized for use by a single patient during a single pregnancy and is available only through authorized Pulsenmore representatives or qualified healthcare organizations. Use of the system does not replace diagnostic in-clinic ultrasound examinations.

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Pulsenmore (NASDAQ, TASE: PLSM), a pioneer in connected home ultrasound, is on a mission to make accessible, patient-driven healthcare a reality.

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© 2026 Pulsenmore Ltd. This is the Pulsenmore global website. The Pulsenmore ES System is cleared for commercial distribution in select markets, including the United States, European Union, United Kingdom, Switzerland, Australia, Brazil, Colombia, and Israel. Product indications and intended use differ by region in accordance with local regulatory approvals.

Last updated May 2026
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