ER Wait Time - Emergency Wait
-47%
$7.55
$3.99
Medical
Free
22-RPM
by twenty two health monitoring services LLC
Description
22-RPM is a Remote Patient Monitoring (RPM) application designed for use exclusively with FDA-cleared medical devices provided by a licensed healthcare provider. The app enables patients to securely transmit vital-sign measurements to their clinician for remote review and follow-up.
Supported Medical Devices (FDA-Cleared)
22-RPM connects only to the following FDA-cleared devices from Shenzhen Viatom Technology Co., Ltd.:
1. Oxyfit Pulse Oximeter
• FDA 510(k) Number: K203812
• Measurements supported: SpO₂ and Pulse Rate
2. BP2/BP2A Blood Pressure Monitor with ECG
• FDA 510(k) Number: K193348
• Measurements supported:
– Systolic & Diastolic Blood Pressure
– Pulse Rate
These devices are supplied directly by healthcare providers and require authorization to pair with the app.
Key Features
• Real-time Device Data Sync
Securely receive supported measurements from the FDA-cleared devices listed above.
• Clinician-Connected Monitoring
Measurements are automatically transmitted to your assigned healthcare provider for review.
• Health Trend Review
Patients can view historical measurements shared by their healthcare provider.
• Secure Cloud Infrastructure
All data is encrypted during transmission and maintained according to healthcare privacy standards.
• Provider-Managed Access
Patient accounts must be created and authorized by a participating clinician.
Medical Disclaimer
22-RPM does not provide medical interpretation, diagnosis, or treatment recommendations.
All measurement values are for informational use only and must be reviewed by a qualified healthcare professional.
Always consult your clinician before making any medical decisions.
Regulatory Jurisdiction Statement
22-RPM supports only the FDA-cleared devices listed above for use within the United States.
Use of these devices outside the United States may require additional regulatory approvals depending on local requirements.
The app does not connect to any other medical devices.
Intended Users
This app is intended for patients who have been provided an FDA-cleared compatible device and login credentials by their healthcare provider.
Supported Medical Devices (FDA-Cleared)
22-RPM connects only to the following FDA-cleared devices from Shenzhen Viatom Technology Co., Ltd.:
1. Oxyfit Pulse Oximeter
• FDA 510(k) Number: K203812
• Measurements supported: SpO₂ and Pulse Rate
2. BP2/BP2A Blood Pressure Monitor with ECG
• FDA 510(k) Number: K193348
• Measurements supported:
– Systolic & Diastolic Blood Pressure
– Pulse Rate
These devices are supplied directly by healthcare providers and require authorization to pair with the app.
Key Features
• Real-time Device Data Sync
Securely receive supported measurements from the FDA-cleared devices listed above.
• Clinician-Connected Monitoring
Measurements are automatically transmitted to your assigned healthcare provider for review.
• Health Trend Review
Patients can view historical measurements shared by their healthcare provider.
• Secure Cloud Infrastructure
All data is encrypted during transmission and maintained according to healthcare privacy standards.
• Provider-Managed Access
Patient accounts must be created and authorized by a participating clinician.
Medical Disclaimer
22-RPM does not provide medical interpretation, diagnosis, or treatment recommendations.
All measurement values are for informational use only and must be reviewed by a qualified healthcare professional.
Always consult your clinician before making any medical decisions.
Regulatory Jurisdiction Statement
22-RPM supports only the FDA-cleared devices listed above for use within the United States.
Use of these devices outside the United States may require additional regulatory approvals depending on local requirements.
The app does not connect to any other medical devices.
Intended Users
This app is intended for patients who have been provided an FDA-cleared compatible device and login credentials by their healthcare provider.
