The WiTOF TOF station is a medical device designed for monitoring the neuromuscular transmission blockade in adult patients. It is intended for use by qualified medical staff, such as intensive care anesthetists, practitioners, or state-recognized anesthetist nurses.
The device consists of a splint that is applied to or may come into contact with the patient. It provides clinical benefits both intra-operatively and post-operatively, allowing practitioners to view and control intraoperative blockade of patients and diagnose residual neuromuscular block.
The WiTOF station is designed for use in a professional health environment, such as hospitals or healthcare centers.
Product Usage Instructions
Ensure that the user manual is kept with the WiTOF at all times.
Before using the WiTOF, read and follow the safety measures described in the user manual.
The WiTOF is intended for use by qualified medical staff who have been trained specifically in the use of this device.
Apply the splint to the patient according to the instructions provided in the user manual.
Turn on the WiTOF station and follow the on-screen instructions for configuration and settings.
To monitor the neuromuscular transmission blockade, ensure that the device is properly calibrated and positioned on the patient.
Interpret the measurements taken by the WiTOF according to clinical judgment and compare them to other clinical observations.
Do not rely solely on the results or values provided by the WiTOF for NMT monitoring. Use them as supplementary information.
For maintenance and preventive maintenance procedures, refer to the service manual available for this device.
For cleaning and disinfection instructions, follow the procedures described in the user manual.
It is important to note that this is a summary of the product information and usage instructions. Please refer to the complete user manual for detailed instructions and precautions.
Expected technical performance
The WiTOF operates as follows:
Electrical stimulation of a patient under anesthesia based on single or repeated impulses lasting 200 microseconds squared and adjustable in intensity from 20 to 60 mA. (Value precision +/- 10%)
Users have access to electrical stimulation modes used in everyday practical clinical situations: TOF, PTC, ATP, DBS, TET, ST.
The muscular response of the thumb or big toe is measured following an electrical stimulation (TOF). The result of this measurement is to detect a movement generated by the muscle concerned and the ratio of the amplitude of the first and last movement during the same stimulation.
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The WiTOF TOF station is a medical device designed for monitoring the neuromuscular transmission blockade in adult patients. It is intended for use by qualified medical staff, such as intensive care anesthetists, practitioners, or state-recognized anesthetist nurses.
The device consists of a splint that is applied to or may come into contact with the patient. It provides clinical benefits both intra-operatively and post-operatively, allowing practitioners to view and control intraoperative blockade of patients and diagnose residual neuromuscular block.
The WiTOF station is designed for use in a professional health environment, such as hospitals or healthcare centers.
Product Usage Instructions
Ensure that the user manual is kept with the WiTOF at all times.
Before using the WiTOF, read and follow the safety measures described in the user manual.
The WiTOF is intended for use by qualified medical staff who have been trained specifically in the use of this device.
Apply the splint to the patient according to the instructions provided in the user manual.
Turn on the WiTOF station and follow the on-screen instructions for configuration and settings.
To monitor the neuromuscular transmission blockade, ensure that the device is properly calibrated and positioned on the patient.
Interpret the measurements taken by the WiTOF according to clinical judgment and compare them to other clinical observations.
Do not rely solely on the results or values provided by the WiTOF for NMT monitoring. Use them as supplementary information.
For maintenance and preventive maintenance procedures, refer to the service manual available for this device.
For cleaning and disinfection instructions, follow the procedures described in the user manual.
It is important to note that this is a summary of the product information and usage instructions. Please refer to the complete user manual for detailed instructions and precautions.
Expected technical performance
The WiTOF operates as follows:
Electrical stimulation of a patient under anesthesia based on single or repeated impulses lasting 200 microseconds squared and adjustable in intensity from 20 to 60 mA. (Value precision +/- 10%)
Users have access to electrical stimulation modes used in everyday practical clinical situations: TOF, PTC, ATP, DBS, TET, ST.
The muscular response of the thumb or big toe is measured following an electrical stimulation (TOF). The result of this measurement is to detect a movement generated by the muscle concerned and the ratio of the amplitude of the first and last movement during the same stimulation.
Distribution: Australia, New Zealand, Papua New Guinea, Fiji
Location: Melbourne, VIC
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