value corresponds to the syringe size in use). The bolus volume infused will be displayed (max. Press C, set volume (in 0.1 ml steps) and confirm with F. If bolus rate is set to zero, the bolus and prime function is switched off. Press C, set new bolus rate and confirm with F. To alter the bolus rate (only when device is stopped):
#Braun perfusor compact user manual code
Double-check the new syringe code while infusion is taking place by pressing F and. Press C, enter a new syringe code and confirm by pressing F. Open the syringe holder, press the syringe code blinks. (During STOP, the infused bolus volume is not added to TOTAL volume.) If applicable, repeat priming with BOL key. 1 ml respectively for 10 seconds can be delivered). Press and hold BOL key again until the line is primed (max. (Prime rate = adjusted bolus rate.) Press F, then BOL once. If syringe type code is correct, press F. If the code does not match the syringe type inserted, see Syringe Tables/-Compatibilities, page 16 ff). to the guides attached underneath the pump. The syringe code displayed must match that of the syringe inserted. The locking lever should snap back on its own. Open the syringe holder, slide the locking lever up and extend the drive unit.Īlign the primed syringe so the flange is positioned in the syringe grip plate, and the top of the plunger is positioned in the syringe pressure plate. 2 seconds and the audible alarm will sound. Note the automatic self-check: All display elements will appear for approx. A rotating pole clamp can be used for a vertical fixation of the Perfusor® For safety purposes attach each device separately to the IV pole. To release, press the black button and lift the pump from the clamp. Push the white key in and slide up.Īttach the Perfusor® compact S from above, clicking it into place. To disconnect, turn the "key” until it is To lock, turn the "key” until it is vertical. Push connecting rod of top pump down into the slot of the pump below until it clicks into place. Special care is required here if a patient is already connected. HF surgical equipment, nuclear spin tomography units, mobile telephones etc.) maintain the recommended protective distances for these devices.įirst press F to access the special functions of the pump (= Select / Enter key).Ī maximum of three devices may be connected together. 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. 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). incompatible disposables may influence the technical specifications.Ĭonnected electrical equipment must comply with the relevant IEC/EN-pecifications (e.g. 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. If staff call is used we recommend to check the equipment once after connecting the pump. Start infusion only if values are corresponding. Possible explosion hazard if used in presence of flammable anaesthetics.Ĭompare displayed value with entered value. 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).
#Braun perfusor compact user manual free
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. Also check the device for possible damage.Ĭonnect to patient only after switching on the device.
Prior to use check audible and visual alarms during self test. Ensure the unit is properly positioned and secured.
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