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General| Manufacturer | GE Healthcare |
|---|---|
| Display | LCD |
| Measurement Principle | Oscillometric |
| Measurement Range (Diastolic) | 20-200 mmHg |
| Pulse Rate Range | 30-240 bpm |
| Operating Modes | Manual, Automatic, STAT |
| Connectivity | USB |
| Measurement Range (Systolic) | 30-260 mmHg |
| Measurement Range (Mean Arterial Pressure) | 20 - 230 mmHg |
| Automatic Measurement Intervals | 1, 2, 3, 5, 10, 15, 30, 60, 90 minutes |
| Power Source | AC Adapter, Rechargeable Battery |
| Alarms | Audible and Visual |
| Data Storage | Up to 1000 measurements |
| Accuracy | ± 3 mmHg |
| Operating Conditions | Temperature: 10°C to 40°C (50°F to 104°F), Humidity: 30% to 85% non-condensing |
| Weight | Approx. 2.5 kg (5.5 lbs) |
Details safety levels indicating potential hazards and their severity.
Details the intended use of the TONOPORT VI for ambulatory BP monitoring.
Discusses biocompatibility and explains the oscillometric measurement process.
Details the functions of each button press on the TONOPORT VI.
Defines symbols used on the equipment and packaging.
Covers battery types (NiMH, alkaline), capacity, and replacement.
Instructions for opening the battery compartment and placing batteries.
Procedure for selecting between NiMH and alkaline batteries.
Cautionary notes for charging rechargeable NiMH batteries.
Describes how to use the VARTA charging unit for batteries.
Explains how to turn the device on and off, as it has no power switch.
Details the device's self-test and battery capacity check upon startup.
Lists initial steps before patient use: clear memory, set time, select protocol, audio signal.
Instructions on how to delete stored blood pressure data.
Guide to choosing between deflation and inflation measurement methods.
Instructions for setting the device's date and time.
Procedure to select between mmHg and kPa units.
Details the three available measurement protocols (P1, P2, P3) and their intervals.
Guide to turn the audio signal on or off.
Explains symbols found on blood pressure cuffs.
Instructions for cleaning single-use and reusable cuffs.
Details on proper cuff application, including safety warnings and accuracy tips.
Connection procedure for single-use cuffs using an adapter.
Steps for conducting an initial measurement to check device readiness.
Guidelines for patients regarding device use, contraindications, and data interpretation.
Overview of buttons, measurement methods, phases, and audio signals.
Instructions for connecting the device to a PC for data output via CASE/CardioSoft.
Details various error codes (E02-E29) and their meanings for troubleshooting.
Steps to install the USB driver and verify PC communication.
Instructions for cleaning the device surface, cuffs, and cables.
Covers technical inspections, calibration, and product disposal guidelines.
Details measuring ranges, accuracy, capacity, interfaces, ambient conditions, and dimensions.
Lists TONOPORT VI accessories and their corresponding part numbers.
Provides manufacturer's declaration on electromagnetic emissions and immunity compliance.
Key points for patients to ensure safe and effective device use and data interpretation.
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