MEDHAB, LLC

Address:1161 Corporate Dr W , Suite 300,Arlington,TX,76006,US

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- Catalog Number : MyNotifi RX - large

Device Description : MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart phone via an app (iOS or android). All data is sent by wifi to a HIPAA controlled server for real time or accumulated time review by the provider. MyNotifiRX can be used to meet the rehabilitation needs of any extremity after injury. It can be used both pre and post-operatively to meet a patient’s rehabilitation needs. It is designed for acute or chronic use especially in patients at high risk for falls. As an added feature it is designed with a fall detection algorithm to alert designated care givers in the case of an emergency independent of a patient’s ability to respond.It is designed with two functions.1) In patients who are evaluated to be at risk for falls, MyNotifi can act as a Fall protection device and monitor. It has a built in algorithm to detect when a possible fall occurs and alerts those that the wearer has designated that an issue has occurred. It is also imbedded with the OTAGO exercise protocol https://www.apta.org/PTinMotion/NewsNow/?blogid=10737418615&id=10737430053 ) which is clinically proven to help prevent falls by improving balance. Long term remote monitoring of patients to assist, adjust, advance or correct exercise regimen is possible. Even more important, it can serve as a means to catch early deterioration of function and signal the need for intervention before an accident occurs.2) With its magnetic strip and extension band, it can be placed on any extremity to record an exercise regimen programmed by the provider. There is a library of over 40 APTA exercises (attach sheet) that can be selected.It is recommended for use in upper extremity patients for both nonoperative and post-operative rehabilitation. MyNotifi is best suited in the lower extremity for the rehab of non surgical patients. The addition of a monitor to measure heart rate and blood oxygenation during exercise adds to patient safety and serves as a measure of physical exertion du

Device Class : 1

Duns Number: 107660874

Premarket Exempt : Yes

Product Code : KQX

Prescription Use : No

Device Count : 1

- Catalog Number : MyNotifi RX - medium

Device Description : MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart phone via an app (iOS or android). All data is sent by wifi to a HIPAA controlled server for real time or accumulated time review by the provider. MyNotifiRX can be used to meet the rehabilitation needs of any extremity after injury. It can be used both pre and post-operatively to meet a patient’s rehabilitation needs. It is designed for acute or chronic use especially in patients at high risk for falls. As an added feature it is designed with a fall detection algorithm to alert designated care givers in the case of an emergency independent of a patient’s ability to respond.It is designed with two functions.1) In patients who are evaluated to be at risk for falls, MyNotifi can act as a Fall protection device and monitor. It has a built in algorithm to detect when a possible fall occurs and alerts those that the wearer has designated that an issue has occurred. It is also imbedded with the OTAGO exercise protocol https://www.apta.org/PTinMotion/NewsNow/?blogid=10737418615&id=10737430053 ) which is clinically proven to help prevent falls by improving balance. Long term remote monitoring of patients to assist, adjust, advance or correct exercise regimen is possible. Even more important, it can serve as a means to catch early deterioration of function and signal the need for intervention before an accident occurs.2) With its magnetic strip and extension band, it can be placed on any extremity to record an exercise regimen programmed by the provider. There is a library of over 40 APTA exercises (attach sheet) that can be selected.It is recommended for use in upper extremity patients for both nonoperative and post-operative rehabilitation. MyNotifi is best suited in the lower extremity for the rehab of non surgical patients. The addition of a monitor to measure heart rate and blood oxygenation during exercise adds to patient safety and serves as a measure of physical exertion during

Device Class : 1

Duns Number: 107660874

Premarket Exempt : Yes

Product Code : KQX

Prescription Use : Yes

Device Count : 1

- Catalog Number : MyNotifi RX - small

Device Description : MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart phone via an app (iOS or android). All data is sent by wifi to a HIPAA controlled server for real time or accumulated time review by the provider. MyNotifiRX can be used to meet the rehabilitation needs of any extremity after injury. It can be used both pre and post-operatively to meet a patient’s rehabilitation needs. It is designed for acute or chronic use especially in patients at high risk for falls. As an added feature it is designed with a fall detection algorithm to alert designated care givers in the case of an emergency independent of a patient’s ability to respond.It is designed with two functions.1) In patients who are evaluated to be at risk for falls, MyNotifi can act as a Fall protection device and monitor. It has a built in algorithm to detect when a possible fall occurs and alerts those that the wearer has designated that an issue has occurred. It is also imbedded with the OTAGO exercise protocol https://www.apta.org/PTinMotion/NewsNow/?blogid=10737418615&id=10737430053 ) which is clinically proven to help prevent falls by improving balance. Long term remote monitoring of patients to assist, adjust, advance or correct exercise regimen is possible. Even more important, it can serve as a means to catch early deterioration of function and signal the need for intervention before an accident occurs.2) With its magnetic strip and extension band, it can be placed on any extremity to record an exercise regimen programmed by the provider. There is a library of over 40 APTA exercises (attach sheet) that can be selected.It is recommended for use in upper extremity patients for both nonoperative and post-operative rehabilitation. MyNotifi is best suited in the lower extremity for the rehab of non surgical patients. The addition of a monitor to measure heart rate and blood oxygenation during exercise adds to patient safety and serves as a measure of physical exertion during

Device Class : 1

Duns Number: 107660874

Premarket Exempt : Yes

Product Code : KQX

Prescription Use : Yes

Device Count : 1

- Catalog Number : Shoe insole size 00 (women 3.0 to 6.5)

Device Description : Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider.

Device Class : 2

Duns Number: 107660874

Premarket Exempt : Yes

Product Code : IKK

Prescription Use : No

Device Count : 1

- Catalog Number : Shoe insole size 0 (women 7.0 to 8.5) (men 5.0 to 6.5)

Device Description : Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider.

Device Class : 2

Duns Number: 107660874

Premarket Exempt : Yes

Product Code : IKK

Prescription Use : No

Device Count : 1

- Catalog Number : Shoe insole size 1 (women 9.0 to 10.5) (men 7.0 to 8.5)

Device Description : footbed wearable device that affords the patient the ability to perform exercise footbed wearable device that affords the patient the ability to perform exercises both at home and in-clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider.

Device Class : 2

Duns Number: 107660874

Premarket Exempt : Yes

Product Code : IKK

Prescription Use : No

Device Count : 1

- Catalog Number : Shoe insole size 2 (women 11.0 to 12.5) (men 9.0 to 10.5)

Device Description : Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider.

Device Class : 2

Duns Number: 107660874

Premarket Exempt : Yes

Product Code : IKK

Prescription Use : No

Device Count : 1

- Catalog Number : Shoe insole size 4 (men 13.0 to 15.0)

Device Description : Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider.

Device Class : 2

Duns Number: 107660874

Premarket Exempt : Yes

Product Code : IKK

Prescription Use : No

Device Count : 1

- Catalog Number : Shoe insole size 3 (women 13.0 to 15.0) (men 11.0 to 12.50)

Device Description : Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in-clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider.

Device Class : 2

Duns Number: 107660874

Premarket Exempt : Yes

Product Code : IKK

Prescription Use : No

Device Count : 1

- Catalog Number : Shoe insole size 0 (women 7.0 to 8.5) (men 5.0 to 6.5)

Device Description : Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider.

Device Class : 2

Duns Number: 107660874

Premarket Exempt : Yes

Product Code : IKK

Prescription Use : No

Device Count : 1