To Next PageTo Next PageWhat does it mean if pressure sensor P1/P2 has been removed on RAUMEDIC?
If the RAUMEDIC Medical Equipment indicates that the pressure sensor P1/P2 has been removed, first confirm if this is the case. If the sensor hasn't been removed, it's likely a sensor defect, so check and replace the sensor if needed.
What does it mean if temperature sensor T1/T2 has been removed on RAUMEDIC?
If your RAUMEDIC Medical Equipment indicates that the temperature sensor T1/T2 has been removed, first confirm if this is the case. If the sensor hasn't been removed, it's likely a sensor defect, so check and replace the sensor if necessary.
What does it mean if pO2 sensor P1/P2 has been removed on RAUMEDIC?
If the RAUMEDIC Medical Equipment indicates that the pO2 sensor P1/P2 has been removed, first confirm if this is the case. If the sensor hasn't been removed, it's likely a sensor defect, so check and replace the sensor if needed.
Device intended for monitoring invasive physiological pressures and patient temperatures.
Specifies where the device can be used, including clinical environments and during transport.
Conditions under which the NeuroSmart can measure and monitor physiological parameters.
Situations where the NeuroSmart should not be used, such as in CT or MRI environments.
Crucial guidelines for safe operation, including user qualifications and proper handling.
Instructions for protecting data and ensuring system security, including software updates.
Explains symbols on the device and their meanings for safe operation and compliance.
Details symbols found on the packaging, indicating handling and storage precautions.
Overview of the device's main and important functions for monitoring and data management.
Steps for initial device setup, including visual inspection and connection diagrams.
Describes the device's interface, including hard keys, touch display areas, and view arrangements.
Guides on initiating measurements, selecting functions, setting limits, and handling data.
Instructions for adjusting system settings like language, scaling, date/time, and graphics.
Details on alarm types, visual/audible indicators, and settings for managing alarms.
How to connect and forward measured data to external devices via analogue outputs.
Information on calculating and using advanced parameters like PRx, ORx, and CPPopt.
Guide on accessing and providing device information to service personnel for error resolution.
Procedures for cleaning the main device unit, including disinfection and sterilization limitations.
Guidelines for cleaning, disinfecting, and sterilizing cables to maintain functionality and safety.
Instructions for cleaning the power adapter, emphasizing avoiding immersion in liquids.
Performance characteristics related to electromagnetic disturbance phenomena and approved deviations.
Guidance on using the device in environments with potential electromagnetic interference and precautions.
Classification of electromagnetic emissions and conformity standards for industrial and hospital use.
Details on immunity test levels for various electromagnetic interference scenarios.
Operator's obligation and recommendations for performing safety checks on medical devices.
Requirements and recommendations for performing measurement checks to ensure accuracy and compliance.
Comprehensive technical specifications including dimensions, power, connectivity, and measurement ranges.
Specifies operating, storage, and transport conditions, including temperature, humidity, and air pressure.
General| Category | Medical Equipment |
|---|---|
| Manufacturer | RAUMEDIC |
| Resolution | 0.1 mmHg |
| Sensor Location | Intracranial |
| Sensor Type | Pressure sensor |
| Usage | Single-use |
| Temperature Range | 10°C to 40°C |
| Dimensions | Varies by component |
| Weight | Varies by component |
| Certifications | CE |
