![]() The Perfusor® compact S is according to IEC/EN 60601-1 resp. HF surgical equipment, nuclear spin tomography units, mobile telephones etc.) maintain the recommended protective distances for these devices. If the equipment is operated in the vicinity of other equipment which may cause high levels of interference (e.g. ➤ The EMC-limits (electro-magnetic compati bility) according to IEC/EN 6 and IEC/EN 6 are maintained. Safety Standards Perfusor® compact S satisfies all safety standards for medical electrical devices in compliance with IEC/EN 60601-1 and IEC/EN 6. The international standard IEC/EN 6 has to be taken into account. The user/operator is responsible for the system configuration if additional equipment is connected. IEC/EN 60950 for data-processing equipment). ➤ Connected electrical equipment must comply with the relevant IEC/EN-pecifications (e.g. incompatible disposables may influence the technical specifications. ➤ Use only compatible combinations of equipment, accessories, working parts and disposables. ➤ Refer to respective manufacturer’s information for possible incompatibilities of equipment resp. ➤ Where several infusion lines are connected on one single vascular access the possibility of their exerting a mutual influence vice-versa cannot be excluded. as caused by change of level) can affect the accuracy of the device. Other components ➤ Variations in pressure (e.g. ➤ If staff call is used we recommend to check the equipment once after connecting the pump. ➤ Do not use the device when service indicator is displayed permanently. Start infusion only if values are corresponding. ➤ Compare displayed value with entered value. ➤ Possible explosion hazard if used in presence of flammable anaesthetics. Observe national specifications and deviations. ➤ Installation in medically used rooms must comply with the appropriate regulations (e.g. ➤ Recommended change of disposables after 24 h (consider national hygiene regulations). ![]() ![]() ➤ Position the infusion line free of kinks. ➤ Select syringe/catheter suitable for use with the intended medical application. Interrupt the connection during syringe changes to prevent incorrect dose delivery. ➤ Connect to patient only after switching on the device. Also check the device for possible damage. ➤ Prior to use check audible and visual alarms during self test. Operation ➤ Ensure the unit is properly positioned and secured. Application only under regularly supervision by specially trained staff. Patient Safety Attention: Consult accompanying documents ! ![]()
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