
The EPSIMED 801 E is a medical device produced by EPSIMED, designed for therapeutic applications. The device is likely used in clinical 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, pulse duration, frequency settings, and safety features to ensure patient comfort and device reliability.
The device is intended for use by trained healthcare professionals. Proper setup, calibration, and adherence to recommended protocols are essential for effective treatment outcomes. Users should follow manufacturer guidelines for electrode placement, session duration, and patient monitoring.
EPSIMED devices generally comply with relevant medical device standards and regulations to ensure safety and efficacy. Users should verify certification marks and ensure the device meets local regulatory requirements.
For detailed technical data, user manuals, and support, visit the official website at www.epsimed.com.
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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