
The EPSIMED 801 E is a medical device produced by EPSIMED, designed for therapeutic applications. The device is likely used in clinical or home care settings, focusing on patient treatment through electrical stimulation or similar modalities.
While detailed technical specifications are not provided in the document snippet, typical parameters for such devices include adjustable intensity levels, treatment modes, and safety features to ensure patient comfort and efficacy.
Standard operating procedures for the EPSIMED 801 E would involve proper device setup, electrode placement, parameter selection according to treatment protocols, and monitoring during use to ensure safety and effectiveness.
The device is expected to comply with relevant medical device regulations and standards, ensuring safety, reliability, and performance. This includes electrical safety standards and possibly certifications for medical use.
Users should follow manufacturer guidelines for device maintenance, cleaning, and storage. Proper training is recommended to optimize treatment outcomes and minimize risks.
INFUSION MODE PUMPING MECHANISM OPTIONAL RATE UNIT FLOW RATE RANGE DRIP RATE RANGE VOLUME LIMIT VOLUME INFUSED DISPLAY FLOW RATE ACCURACY DRIP RATE ACCURACY PURGE RATE BOLUS MODE BOLUS RATE DRIP SENSOR OCCLUSION PRESSURE AIR-IN-LINE DETECTION IVSET MANAGEMENT FLOW RATE CALIBRATION POWER SOURCE PERISTALTIC FINGER PUMP INFRARED OPTOELECTRONIC DETECTION "PRESSURE DETECTION DEVICE WITH "AIR-IN-LINE DETECTION DEVICE WITH UP TO 20 IV SETS OF CUSTOMERS' BRAND CAN &BE ADDED, STORED AND DELETED IN MEMORY, CONVENIENT FOR OPERATION AFTER CALIBRATION. BLUE LCD WITH HIGH BRIGHTNESS RECHARGEABLE Nl-MH BATTERY:...
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