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General| Control | Digital |
|---|---|
| Portability | Portable |
| Category | Medical Equipment |
| Intended Use | Recovery, Rehabilitation |
| Technology | Pneumatic Compression |
| Pressure Range | 20-110 mmHg |
| Timer | Adjustable |
| Treatment Time | Adjustable |
What the NormaTec PULSE Recovery System is used for.
Potential risks and benefits associated with using the system.
Overview of the main control unit and its components.
Identification of the NormaTec hose and its connectors.
Details of the leg attachment and its zones.
Details of the arm attachment and its zones.
Details of the hip attachment and its zones.
Identification of the power supply components.
Step-by-step guide to setting up the NormaTec PULSE system.
Instructions on how to adjust session pressure and duration.
How to initiate a recovery session.
Description of the massage pattern and session experience.
Steps for ending a session and disconnecting the system.
How to pause or stop an ongoing session.
Procedure for powering down the system.
Guide to using the Zone Boost feature for targeted intensity.
Information on the device's internal battery and charging.
How to configure the pause duration between cycles.
Steps to change between Pulse and Sequential massage modes.
Method to enable or disable specific zones in the attachments.
Instructions for cleaning the control unit and attachments.
Overview of system maintenance requirements.
Guidance on proper storage of the device.
Information on ordering replacement parts.
Details about the rechargeable lithium-ion battery.
Physical dimensions of the NormaTec PULSE unit.
Weight specification for the NormaTec PULSE unit.
Electrical specifications for the device.
Details and warnings for the AC-DC power adapter.
Operating temperature range for the device.
Storage temperature range for the device.
Operating relative humidity limits.
Storage relative humidity limits.
Atmospheric pressure limits for storage and transport.
Atmospheric pressure limits during operation.
Important precautions regarding EMC for medical devices.
Information on RF emissions and compliance.
Details on the device's immunity to electromagnetic disturbances.
Guidance on using the device in specific electromagnetic environments.
Recommended distances for RF devices to avoid interference.
Classification regarding protection against electric shock.
Type of protection against electric shock (BF applied part).
IP rating for protection against solids and liquids.
Warning about use with flammable anesthetic mixtures.
Indicates the device's operational mode.
Solutions for when the device fails to power on.
Troubleshooting steps for non-inflating attachments.
Solutions if the device stops pumping during use.
How to address air leak error messages.
Guidance for low battery indications.
Details of the warranty for the control unit.
Details of the warranty for attachments and accessories.
Instructions for returning or exchanging products.
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