BIO-MED DEVICES MVP-10 Instruction Manual Download Page 29 | Manualshive

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Summary of Contents for MVP-10

Page 1: ...O MED DEVICES MVP 10 NEONATAL PEDIATRIC VENTILATOR INSTRUCTION MANUAL Catalog 2050 Rev 042916 BIO MED DEVICES INC 61 SOUNDVIEW ROAD GUILFORD CT 06437 800 224 6633 FAX 203 458 0440 www biomeddevices co...

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Page 3: ...INSTALLATION CONSIDERATIONS 15 A EQUIPMENT REQUIRED 15 B SUPPLY GAS 15 C MOUNTING BRACKET 15 D PATIENT CIRCUIT 15 E OPTIONAL EQUIPMENT 15 IV VENTILATOR SET UP 17 A CONNECTION OF GAS SUPPLY 17 B CONNE...

Page 4: ...FREE STANDING AND DESIGNATED BY AN MR CONDITIONAL LABEL AND AN M AS A SUFFIX TO THE SERIAL NUMBER WHEN USING THE MVP 10 MRI VENTILATOR IN AN MRI ENVIRONMENT THE FOLLOWING PRECAUTIONS MUST BE TAKEN THE...

Page 5: ...SN Serial Number REF Catalog Number Authorized Representative in the European Community The CE mark displayed on this product signifies that this device is in compliance with the European Medical Devi...

Page 6: ...3...

Page 7: ...Two 2 supply hoses 1 4 ID x 3 8 OD x 10 long with attached DISS fittings one hose for air and one for oxygen Bracket for mounting MVP 10 to column Instruction Manual and Warranty Card Infant Test Lung...

Page 8: ...the blender bracket together and separate the two halves Wrap the two halves around the pole and loosely secure the bracket to the pole below the ventilator using the two screws Be sure the two pins...

Page 9: ...and hoses supplied with the instrument Nor does the warranty cover abuse or misuse of the instrument or damage due to unauthorized servicing If service is required the instrument must be properly pack...

Page 10: ...stance or system malfunction Breathing through the negative pressure relief valve requires a greatly increased work of breathing and only air is provided A situation in which the patient is breathing...

Page 11: ...The high pressure alarm level should never be set above the lowest relief valve setting Do not continue using a ventilator which has been significantly impacted or abused Volume limited ventilators sh...

Page 12: ...ssure limitation with or without Positive End Expiratory Pressure PEEP Intermittent Positive Pressure Ventilation IPPV Intermittent Mandatory Ventilation IMV Continuous Positive Airway Pressure CPAP C...

Page 13: ...ned by INSP TIME and EXP TIME control settings These settings are approximate time reference points which are repeatable within 5 For greater accuracy an external monitoring device may be used The tid...

Page 14: ...me limited The pressure developed in the patient s airway depends upon the total system patient compliance and the tidal volume being administered When the PIP control is set at a pressure above the p...

Page 15: ...provided past the patient WYE allowing the patient to inhale from this flow while maintaining the airway at the pre set constant positive pressure b Continuous Flow or Constant Oxygen Administration C...

Page 16: ...LOGIC CIRCUIT CYCLE CPAP SWITCH PEEP CPAP CONTROL EXP TIME CONTROL MAX PRESSURE CONTROL INSP TIME CONTROL EXPIRATION VALVE CONNECTION GAUGE CONNECTION PATIENT CONNECTION ADJUSTABLE RELIEF VALVE TWO WA...

Page 17: ...system in liters minute CONNECTIONS Rear Panel 11 AIR Connection to pressurized source of clean dry oil free air 50 5 PSI Mates with female DISS air fitting 12 POWER OXYGEN Connection to pressurized s...

Page 18: ...t PATIENT connection user adjustable to open between a maximum pressure of 80 cm H2O 10 cmH2O when turned fully clockwise to a minimum of 10 cmH2O 5 cmH2O when turned fully counterclockwise PEEP CPAP...

Page 19: ...is installed externally and may be adjusted to vent pressures between 70 cm H2O 10 cmH2O and 10 cm H2O 5 cmH2O INSP TIME and EXP TIME control settings are calibrated at sea level and 20o C ATPD using...

Page 20: ...gic and may render the time cycling inoperative The MVP 10 will operate with a supply pressure outside of the 50 5 PSI 345 34 5 kPa range but accuracy of settings may be impaired In no case should a s...

Page 21: ...nd or low T connected to Gauge line A Humidifier or Pressure Alarm connection can affect system compliance Connecting hoses and water level in the Humidifier should be arranged so that system complian...

Page 22: ...es without flow restricting devices e g flowmeter valve A 50 PSI 345 kPa supply must always be connected to the POWER OXYGEN fitting for proper operation of the pneumatic logic controls Hose fittings...

Page 23: ...rovided by a heated flow through humidifier or artificial nose If a Humidifier is not used connect hose of patient circuit directly to ADJUSTABLE RELIEF VALVE e Connect patient port of WYE to a test l...

Page 24: ...MULTIPLICATION FACTOR from CHART C or by use of slide rule Set flow rate controls for this total flow STEP 4 Set CYCLE CPAP switch in CYCLE position STEP 5 For oxygen concentration FIO2 other than air...

Page 25: ...otal Flow VI 10 ml 0 5 sec Total Flow VI 20 ml sec 1 2 liters min From CHART A For 60 oxygen concentration Oxygen Flow VIO2 600 ml min 0 6 liters min Air Flow VAir 600 ml min 0 6 liters min STEP 6 Att...

Page 26: ...pliance of the system by increasing total flow In the previous example 5 ml must be supplied for the compliance in the system as well as the prescribed 10 ml tidal volume for the patient Therefore adj...

Page 27: ...lock ring to secure adjusting cap Adjust PIP control until the desired pressure limit is seen during inspiration Note that the PIP level is somewhat affected by the flow rate It should be set with th...

Page 28: ...by setting flow so that the pressure gauge reading does not drop during patient inhalation STEP 4 For oxygen concentration other than air or 100 oxygen set by adjusting integral flow rate controls acc...

Page 29: ...24...

Page 30: ...3 5 3 2 30 9 8 1 46 8 5 5 2 5 53 11 6 5 4 5 31 4 3 5 0 5 46 9 5 6 5 3 53 13 5 8 5 5 31 8 7 1 46 11 7 5 3 5 53 15 9 6 31 11 5 10 1 5 46 12 5 8 5 4 53 16 9 5 6 5 32 3 5 3 0 5 46 14 9 5 4 5 54 6 3 5 2 5...

Page 31: ...5 8 59 15 5 8 7 5 65 16 7 9 72 14 5 9 59 16 5 8 5 8 65 17 7 5 9 5 72 15 5 5 5 10 59 17 5 9 8 5 65 18 8 10 73 11 5 4 7 5 61 6 3 3 66 3 5 1 5 2 73 13 4 5 8 5 61 8 4 4 66 7 3 4 73 14 5 5 9 5 61 9 4 5 4 5...

Page 32: ...5 5 80 10 2 5 7 5 93 11 1 10 80 12 3 9 94 6 5 0 5 6 80 13 5 3 5 10 94 7 0 5 6 5 81 8 5 2 6 5 95 7 5 0 5 7 81 10 5 2 5 8 95 8 0 5 7 5 81 12 5 3 9 5 95 8 5 0 5 8 82 4 5 1 3 5 96 9 0 5 8 5 82 6 5 1 5 5...

Page 33: ...2 14 4 4 5 71 1 2 6 8 13 5 5 0 67 1 1 6 4 12 8 5 5 63 1 1 6 1 12 1 6 0 60 1 0 5 8 11 5 7 0 55 94 5 2 10 5 8 0 50 86 4 8 9 6 9 0 46 79 4 4 8 8 10 0 43 74 4 1 8 2 11 0 40 69 3 8 7 7 12 0 38 65 3 6 7 2...

Page 34: ...180 25 2 4 Insp Time Exp Time Mult Factor 1 8 0 6 33 3 1 6 0 8 37 5 1 44 96 41 7 1 2 1 2 50 96 1 44 62 5 0 8 1 6 75 0 6 1 8 100 48 1 92 125 0 4 2 0 150 34 2 06 176 0 3 2 1 200 27 2 13 225 30 2 Insp Ti...

Page 35: ...proach setting by turning knob in a clockwise direction Humidifier should have low compliance and water maintained at a high level to minimize compliance Expiration Valve must be positioned with diaph...

Page 36: ...flow rate is changed the PIP and PEEP CPAP levels should be checked When a compressor is used as the power source steps should be taken to filter and dehumidify the room air before introducing it int...

Page 37: ...and AIR fittings Hand tightening of these fittings is sufficient Do not over tighten with a wrench as the fittings could be damaged Never connect a water supply to these fittings Use only clean dry oi...

Page 38: ...itch to CYCLE PIP full CCW PEEP PRESSURE full CW TOTAL FLOW of 6 LPM INSPIRATORY TIME 2 sec EXPIRATORY TIME 1 sec Manometer should read 70 5 cm during inspiratory Turn PIP knob clockwise until pressur...

Page 39: ...conds C CALIBRATION The accuracy of the instrument s indicators and controls should be retained over its life as long as it has not been subject to abuse The calibration of the pressure gauge flow met...

Page 40: ...For units used infrequently a maximum of 3 years between factory service is recommended Calibration may be periodically verified by qualified personnel following prescribed checkout procedures The ann...

Page 41: ...A AUTHORIZED REPRESENTATIVE IN THE EUROPEAN COMMUNITY Bio Med Devices Official Agent in Europe is Medical Market I N T AB Sehlstedtsgatan 6 115 28 Stockholm Sweden Telephone 46 08 767 70 00 Fax 46 08...

Page 42: ...the area of interest is in the same area or relatively close to the position of the device Therefore it may be necessary to optimize MR imaging parameters for the presence of this device Additional r...

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