Medtronic Minimed, Inc.

Pentair Pool Products, Inc.

Afshin Bazargan

Pablo Vazquez

Juan M Alderete, Jr

Jacob E Pananen

R Marie Tieck

Hsiao-Yu S Kow

Salman Monirabbasi

Adam S Trock

Ian B Hanson

EJMar Fonacier

Andrew E Weaver

Patrick E Weydt

Hans K Wenstad

Samuel Finney

Seung C Shin

Sheldon B Moberg

Kevin Lee Bokelman

Chad Srisathapat

Sarnath Chattaraj

Guangping Zhang

Seth N Kazarians

Fatemeh Delijani

Jalal Elidrissi

Edmond W Yu

Zhaleh Lotfi

Paul F Bente, Iv

Daniel Steven Kline

Paul S Cheney, Ii

Paul H Kovelman

Kirk Andrew Allen

Steven Masterson

Anthony C Ng

Mark Lin

Anuradha Biswas Bhatia

Andrew B Nguyen

David Law

Maria C LoVerme

Eric M Lorenzen

Yuxiang Zhong

Matthew William Yavorsky

Edgardo C Halili

Steve Masterson

Arsen Ibranyan

Ali Dianaty

Hubert K Yeung

Yongbo Wang

Benjamin A Grover

Susan McConnell Montalvo

Ulrich H Rankers

Hsi Chung Fusselman

Bozhil Makaveev

Dan Kline

Sherif M Ali

Vaughn S Sakae

Michael Ivey

Jennifer L Wagner

Virgilio Macion

Ben Wu

Jinghua Chen

Juan M Alderete

Susan Mcconnell Montalvo

Paul Bente

Jr Juan M Alderete

Paul F Iv Bente

A medicine injection pen includes a body, a drive member, a cartridge housing, and a medicine cartridge retained within the cartridge housing. The drive member is configured to move relative to the body and the medicine cartridge defines an interior volume configured to retain a liquid medicine. The drive member is configured to translate a piston within the interior volume toward a dispensing end of the medicine cartridge to dispense at least some of the liquid medicine. The medicine cartridge also includes an insertion port configured to receive a medicine dispensing element therethrough for dispensing a liquid medicine into the interior volume to replace at least some of the liquid medicine dispensed through the dispensing end. Dispensing of the liquid medicine into the interior volume of the medicine cartridge applies a fluid pressure to the piston to translate the piston away from the dispensing end of the medicine cartridge.

Injection pens for medicine administration

Embodiments are provided for dynamic management of charge. The techniques may involve charging, using a first charging rate, an energy storage element to an intermediate state of charge, wherein the energy storage element is interchangeable with an in-use energy storage element. The techniques may further involve responsive to at least an identification of an anomalous condition of a device powered by the in-use energy storage element, the anomalous condition resulting in the in-use energy storage element being discontinued from use, charging, using a second charging rate, the energy storage element to a target state of charge, wherein the second charging rate is different from the first charging rate.

Dynamic management of charge

A method and apparatus for a connection interface between a reservoir or syringe, infusion set tubing, and an infusion pump is provided. The reservoir, a base and a cap are connected to form an integrated unit that is capable of being inserted and secured in an infusion pump housing. The cap and the infusion pump are each provided with at least one sensor or at least one detectable feature, arranged to interact with at least one corresponding detectable feature or sensor on the other of the cap and infusion pump device, to detect one or more of the presence, position or other characteristic of the cap when the cap is aligned or coupled with the infusion pump housing. The detectable feature and sensor may be magnetic, RF, mechanical, optical or any combination.

Smart connection interface

Devices, systems, and techniques for automatic network configuration based on biometric authentication are described herein. In one example, one or more processors may obtain first biometric data derived from one or more sensor signals generated by one or more sensors of a first device coupled to a user. The one or more processors may obtain second biometric data derived from one or more sensor signals generated by one or more sensors of a second device. The one or more processors may compare the first biometric data and the second biometric data, determine that the second device is coupled to the user based on the comparison, and establish a communication link with the second device based on the determination that the second device is coupled to the user.

Automatic network configuration based on biometric authentication

Infusion devices, systems, and related operating methods are provided. A method of detecting an anomalous condition with respect to a fluid path involves providing energy to an actuation arrangement to produce actuation, wherein the actuation arrangement is coupled to a plunger configured to deliver fluid via the fluid path, monitoring an orientation of the actuation arrangement using a sensing arrangement, and detecting an anomalous condition based on the orientation of the actuation arrangement.

Methods and devices for occlusion detection using actuator sensors

A method for automatically configuring a medical device with user-specific configuration data includes determining, by a first medical device, that the first medical device is being removed from service, wherein the first medical device was previously placed into service to provide therapy to a patient in accordance with user-specific configuration data stored on the first medical device, and wherein the first medical device is to be replaced with a second medical device that is a replacement medical device for the first medical device, and causing, by the first medical device in response to determining that the first medical device is being removed from service, configuration of the second medical device to provide therapy to the patient in accordance with the user-specific configuration data, wherein causing configuration of the second medical device comprises communicating the user-specific configuration data toward the second medical device.

Automatic configuration of user-specific data based on removal from service

Embodiments are provided for dynamic management of charge. The techniques may involve obtaining an estimated readiness time for an energy storage element, obtaining a target state of charge for the energy storage element, calculating an estimated charging time based at least in part on a difference between the target state of charge and a current state of charge, using a first charging rate to charge the energy storage element to an intermediate state of charge, and responsive to determining the amount of time remaining before reaching a second estimated readiness time is less than an updated estimated charging time to charge the energy storage element at the intermediate state of charge to the target state of charge, using a second charging rate to charge the energy storage element to the target state of charge, wherein the second charging rate is greater than the first charging rate.

Techniques disclosed herein relate generally to notification generation in a medical device system. In some embodiments, the techniques involve generating a first notification via a medical application executing on a first device, determining that the first notification was not acknowledged within a predetermined time frame, and causing generation of a second notification at a medical device carried by a user to notify the user that the first notification has not been acknowledged.

Backup notifications in a medical device system

A method for automatically configuring a medical device with user-specific configuration data includes obtaining, by a charger device from one or more server computing devices, user-specific configuration data stored on a first medical device that is configured to provide therapy to a patient in accordance with the user-specific configuration data, and causing, by the charger device, configuration of a second medical device based on communicating the user-specific configuration data to the second medical device while the second medical device is being charged by the charger device, wherein the second medical device is a replacement device for the first medical device.

Automatic configuration of user-specific data based on networked charger devices

Infusion systems including infusion devices and consumables and related operating methods are provided. An exemplary consumable component includes a housing, a reservoir contained within the housing, a pumping mechanism for dispensing a fluid from the reservoir, and a readable element associated with the housing. The readable element maintains calibration data characterizing a relationship between delivery of the fluid and actuation of the pumping mechanism.

Infusion system consumables and related calibration methods

Embodiments are provided for dynamic management of charge. A method involves obtaining an estimated readiness time for an energy storage element, obtaining a target state of charge for the energy storage element, calculating an estimated charging time based at least in part on a difference between the target state of charge and a current state of charge, using a first charging rate to charge the energy storage element to an intermediate state of charge responsive to determining a time difference between the estimated readiness time and a first time is greater than the estimated charging time, maintaining the energy storage element at the intermediate state of charge, and responsive to determining a time difference between the estimated readiness time and a second time is less than the estimated charging time, using a second charging rate to charge the energy storage element to the target state of charge.

A method for automatically configuring a medical device with user-specific configuration data includes determining, by a first medical device, that the first medical device is being placed into service to provide medical therapy to a patient, wherein the first medical device is a replacement medical device for a second medical device that was previously placed into service to provide medical therapy to the patient in accordance with user-specific configuration data stored on the second medical device, communicating, by the first medical device, data indicative of the first medical device being placed into service, after communicating the data indicative of the first medical device being placed into service, obtaining, by the first medical device, the user-specific configuration data stored on the second medical device, and configuring, by the first medical device, the first medical device to provide therapy in accordance with the obtained user-specific configuration data.

Automatic configuration of user-specific data based on placement into service

Infusion devices, systems, and related operating methods are provided. A method of detecting an occlusion in a fluid path involves a control module of an infusion device operating a driver module to provide energy to an actuation arrangement to achieve a commanded actuation state, wherein the actuation arrangement is coupled to a plunger configured to deliver fluid via the fluid path, obtaining a measured actuation state of the actuation arrangement via a sensing arrangement, and detecting an occlusion condition based on a relationship between the commanded actuation state and the measured actuation state.

Medical devices and methods and apparatuses for identifying fluids in a conduit of a device are provided. An exemplary medical device includes a reservoir for holding a fluid and a conduit for dispensing the fluid from the reservoir. Further, the medical device includes a spectroscopy device for examining the fluid.

Infusion devices and fluid identification apparatuses and methods

Infusion devices, systems, and related operating methods are provided. A method of detecting an anomalous condition with respect to a fluid path based on operation of an actuation arrangement configured to deliver fluid via the fluid path involves providing input power to the actuation arrangement to produce actuation of the actuation arrangement, identifying an active amount of actuation of the actuation arrangement concurrent to the input power being provided to the actuation arrangement, disabling the input power to the actuation arrangement, identifying a passive amount of actuation of the actuation arrangement after disabling the input power to the actuation arrangement, and detecting the anomalous condition based on a relationship between the active amount and the passive amount.

Growing community of inventors

Simi Valley, CA, United States of America

Afshin Bazargan