Sonitor Introduces SonitorBLU™ and SonitorMOBILE™

New Tiered Product Line Opens Low-Cost RTLS Entry Point for Asset Tracking “Phone as an RTLS Tag”

Sonitor® Technologies today announced expansion of its market leading Sense™ platform with SonitorBLU, a proprietary Bluetooth Low Energy (BLE) solution for use cases when zonal accuracy is required, and SonitorMOBILE, a location visibility platform for positioning smart devices, combining Sonitor’s ultrasound technology with BLE to provide best-in-class accuracy, effectively turning a smart phone into an RTLS tag. The company made the announcement at the HIMSS Global Health Conference where it is exhibiting from April 18-20.

Sonitor’s new portfolio offers a tiered approach to the challenges faced by healthcare providers. These range from simple asset tracking to more demanding applications that require speed and accuracy such as patient flow and clinical workflow, as well as the critical need to ensure staff safety. As with Sense, these new products offer advanced analytics for workflow insights, and appropriate staffing assignments that help increase hospital capacity and improve patient and staff satisfaction.

“Sonitor is excited to invite healthcare providers, technology partners and all HIMSS attendees to our booth where we will be showcasing the SonitorBLU, Sonitor Sense and SonitorMOBILE suite of products,” said Matt Crane, Chief Commercial Officer, North America/CEO, Sonitor Inc. “In addition, we have recently expanded our team of clinical and technology experts to customize Sonitor’s solutions to meet customers’ strategic objectives and budgets.”

With SonitorBLU, hospitals have an easy-to-install platform to address use cases such as asset tracking when near real-time data flow is sufficient. With no cabling, installation is simple and fast, and the system can be up and reporting locations in less than a day. SonitorMOBILE, combines Sonitor’s patented ultrasound technology, SonitorULE™, and BLE to provide centimeter level accuracy with refresh rates of 1-2 seconds, to “move at the speed of a nurse™,” for highly demanding use cases.

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”