Masimo Corporation

Cercacor Laboratories, Inc.

Masimo Laboratories, Inc.

Willow Laboratories, Inc.

Masino Corporation, Inc.

Mastmo Corporation

Carcacor Laboratories, Inc.

Ammar Al-Ali

Massi Joe E Kiani

Walter M Weber

Mohamed Kheir Diab

Yassir Kamel Abdul-Hafiz

Bilal Muhsin

Chad A DeJong

Kevin Forrest

Keith Ward Indorf

Marcelo M Lamego

Sujin Hwang

Valery G Telfort

Robert A Smith

Nicholas Evan Barker

Anand Sampath

David Dalke

John Schmidt

Eric Karl Kinast

Michael O'Reilly

Benjamin C Triman

Mohammad Usman

Stephen Scruggs

David R Tobler

Robert James Kopotic

Omar Ahmed

Sung Uk Lee

Eric Yang

Lorenzo Cazzoli

Anmol Majmudar

Eugene E Mason

William Jack MacNeish, Iii

Ryan Timothy McHale

Peter Scott Housel

Michael Petterson

John Graybeal

Jerome Novak

Ronald Coverston

Paul Ronald Jansen

Dimitar Dimitrov

Phi Trang

Prashanth Iyengar

Faisal Mahmood Kashif

Predrag Pudar

Virginia Thanh Ta

Steven Egge

Kesu Wang

Roger Wu

Kirby Clark Dotson

Gregory A Olsen

Philip Perea

Jad Adel Wafeeq

Richard Priddell

Gene Mason

Pierre De Malliard

Bowen Zhao

Rick Fishel

Cornelius Raths

Ronald Keith Rumbaugh, Ii

Nadeesha O Ranasinghe

Chris Kilpatrick

Peter Sunghwan Min

Rex J McCarthy

Michael Lee

Jim Litchfield

Sebastian T Frey

Don Carothers

Hyejin Cho

Sungwhan Cha

Christian Schulz

Gilberto Sierra

Boris Popov

Kun Han Kim

Lorenzo Cazzoll

Philip B Trinh

Atiyeh Ghoreyshi

Paul Martek

Chris Schulz

Garrick Maurer

James P Coffin

Faisal Kashif

Steve Coon

Evan Thomas Fullerton

Swapnil Sudhir Harsule

Marc Pelletier

Greg A Olsen

Thomas J Gerhardt

Julian M Goldman

Mike A Mills

Val E Vaden

Balaji Chandrasekaran

Fahad Abdulrahman Alaql

Yuying Song

Jinwoo Kim

Alejandro Garfio

James P Welch

Joel S Fechter

Divya Srinivasan Breed

Prashanth Rengaswamy Chandran

Jerome J Novak, Jr

A first medical device can receive a physiological parameter value from a second medical device. The second physiological parameter value may be formatted according to a protocol not used by the first medical device such that the first medical device is not able to process the second physiological parameter value to produce a displayable output value. The first medical device can pass the physiological parameter data from the first medical device to a separate translation module and receive translated parameter data from the translation module at the first medical device. The translated parameter data can be processed for display by the first medical device. The first medical device can output a value from the translated parameter data for display on the first medical device or an auxiliary device.

System for displaying medical monitoring data

A blood pressure monitor configured to removably mount to a cuff in a substantially symmetrical position with respect to a width of the cuff can include a housing defining an interior, a first port, and a second port. The first port can: secure to a first prong of the cuff when the cuff is mounted in a first orientation; receive and secure to a second prong of the cuff when the cuff is mounted in a second orientation; and enable fluid communication between the interior and at least one of a first fluid passage within the first prong and a second fluid passage within the second prong. The second port can: secure to the second prong of the cuff when the cuff is mounted in the first orientation; and receive and secure to the first prong of the cuff when the cuff is mounted in the second orientation.

Blood pressure cuff

A localized sound projection system can coordinate the sounds of speakers to simulate the placement of an auditory cue in a 3D space. The system can include a plurality of speakers configured to output auditory signals and a sound localization controller configured to control the plurality of speakers to coordinate the auditory signals to simulate an origination location of a patient alarm. The sound localization controller can determine adjusted auditory signals and control a plurality of speakers to output the plurality of adjusted auditory signals. A method for dynamically controlling speaker settings in a medical environment can include determining volume settings corresponding to a speaker, monitoring a level of ambient noise corresponding to a room of a patient, controlling the volume settings of the speaker to reduce or increase a sound level output of a speaker. A patient monitoring system can be configured to physically manipulate medical devices in response to audible commands. The system can receive a plurality of vocal commands from a user and can manipulate various settings after confirmation from a user.

Localized projection of audible noises in medical settings

A system for remotely monitoring and managing health statuses of a plurality of users includes software instructions storable on a memory device usable by a computing device, the software instructions causing a hardware processor of the computing device to receive a plurality of sets of health-related information from a plurality of mobile computing devices of a plurality of users. The health-related information includes physiological information derived from wearable devices of the users indicative of an onset of symptoms associated with an infection, contact tracing data, and diagnosis data. The hardware processor determines exposure levels based on at least the contact tracing data, and determines user-specific risk states based on physiological information, diagnosis data, and exposure levels.

Wearable device for monitoring health status

The present disclosure relates to physiological monitoring to determine the depth of consciousness of a patient under sedation. The monitor includes an EEG sensor and a depth of consciousness monitor. The depth of consciousness monitor can utilize treatment data, such as patient data and/or drug profile information with an EEG signal to determine whether the patient is adequately sedated.

Depth of consciousness monitor

Various connector and sensor assemblies are described. In some embodiments, the connector and sensor assembly comprises a connector and a sensor assembly. The connector can have an opening that has a first surface and second surface that are opposite each other. The connector can have a plurality of retractable electrical connectors that extend from the first surface and a lock structure that is located on the second surface. The sensor assembly is comprised of a body portion and a proximal end. The proximal end has a top side and a bottom side. The top side includes a plurality of electrical contacts that is configured to interact with the plurality of retractable electrical connectors. The bottom side includes a key structure that is configured to interact with the lock structure in the connector.

Pogo pin connector

A wearable device for a noninvasive measurement of a user's body temperature can include a housing, a first substrate coupled to the housing and having an opening, a second substrate coupled to the first substrate and configured to secure to skin of a user, a mounting frame enclosed by the housing and the first substrate, a circuit board secured by the mounting frame, a temperature sensor coupled to the circuit board and configured to determine a body temperature of the user, and a thermally conductive probe. The thermally conductive probe is secured by the mounting frame and positioned proximate to the first temperature sensor. The thermally conductive probe extends at least partially through the opening in the first substrate and transmits a thermal energy from a portion of the user's skin to the first temperature sensor.

Wearable device for noninvasive body temperature measurement

Band

A physiological parameter system has one or more parameter inputs responsive to one or more physiological sensors. The physiological parameter system may also have quality indicators relating to confidence in the parameter inputs. A processor is adapted to combine the parameter inputs, quality indicators and predetermined limits for the parameters inputs and quality indicators so as to generate alarm outputs or control outputs or both.

Physiological parameter system

A regional oximetry pod drives optical emitters on regional oximetry sensors and receives the corresponding detector signals in response. The sensor pod has a dual sensor connector configured to physically attach and electrically connect one or two regional oximetry sensors. The pod housing has a first housing end and a second housing end. The dual sensor connector is disposed proximate the first housing end. The housing at least partially encloses the dual sensor connector. A monitor connector is disposed proximate a second housing end. An analog board is disposed within the pod housing and is in communications with the dual sensor connector. A digital board is disposed within the pod housing in communications with the monitor connector.

Regional oximetry pod

A regional oximetry system comprises a pod having a pod housing defining a sensor end and an opposite monitor end. A dual sensor connector is in electrical communication with the sensor end of the pod housing. A monitor connector is in electrical communication with the monitor end of the pod housing. An analog board is disposed within the pod housing and is in electrical communications with the dual sensor connector. The analog board receives and digitizes sensor signals from at least one optical sensor plugged into the dual sensor connector. A digital board is disposed within the pod housing and in electrical communications with the analog board and the monitor connector. A digital signal processor (DSP) is mounted on the digital board and implements a regional oximetry signal processor so as to receive digitized sensor signals from the analog board, derive regional oximetry parameters from the digitized sensor signals and communicate the regional oximetry parameters to the monitor connector for display on an attached monitor.

Regional oximetry signal processor

A monitoring system can be configured to monitor activities or actions occurring in clinical settings, such as hospitals. The monitoring system can improve patient safety. The system can use visual and/or other tracking methods. The system can detect and/or identify people in a clinical setting. The system can also track activities of the people, for example, to improve adherence to hygiene protocols.

System and method for monitoring clinical activities

An optical physiological sensor can be integrated into a wearable device and can comprise a substrate having an optical center, a first emitter group of light emitting diodes (LEDs) positioned adjacent to the optical center of the substrate and spaced at an offset from the optical center, a second emitter group of LEDs positioned adjacent to the optical center of the substrate at an offset to the optical center and spaced at an offset from the optical center opposite the first emitter group of LEDs relative to the optical center, and a plurality of detectors arranged in a spatial configuration that surrounds the first and the second emitter group. Each of the plurality of detectors can be positioned on the substrate a same distance away from the optical center of the substrate.

Wearable device with physiological parameters monitoring

The present disclosure includes a medical monitoring hub as the center of monitoring for a monitored patient. The hub includes configurable medical ports and serial ports for communicating with other medical devices in the patient's proximity. Moreover, the hub communicates with a portable patient monitor. The monitor, when docked with the hub provides display graphics different from when undocked, the display graphics including anatomical information. The hub assembles the often vast amount of electronic medical data, associates it with the monitored patient, and in some embodiments, communicates the data to the patient's medical records.

Medical monitoring hub

The present disclosure describes embodiments of a patient monitoring system and methods that include the measure and display of hemoglobin statistics. In an embodiment, total hemoglobin trending is displayed over a period of time. Statistics can include frequency domain analysis, which may be unique for each patient monitored. The total hemoglobin trending and/or statistics can further be used to help control the treatment of a patient, such as being used to control IV administration.

Hemoglobin display and patient treatment

Growing community of inventors

San Juan Capistrano, CA, United States of America

Ammar Al-Ali