7
PHYSIO-PORT / PHYSIO-PORT AS
A8136 Revision A
General Information
PAR Medizintechnik GmbH & Co. KG
Sachsendamm 6
10829 Berlin
Germany
Tel. +49 30 235 07 00
Fax +49 30 213 85 42
The country of manufacture is indicated on the device label.
Страница 1: ...PHYSIO PORT and Variant PHYSIO PORT AS Recording System for Long Term Blood Pressure Measurements and Pulse Wave Analyses Firmware Version 3 0 Operator s Manual A8136 ENG Revision A...
Страница 2: ...ns This manual was created with great care In case you find details which do not correspond to the system please inform us so that we can resolve the discrepancies as soon as possible Due to continuin...
Страница 3: ...Basic Facts about the Battery Supply 14 3 2 Inserting Batteries 15 3 3 Selecting the Energy Source 15 3 4 Charging NiMH batteries 15 3 5 Akkus mit dem Ladeteil VARTA laden 16 3 6 Switching PHYSIO POR...
Страница 4: ...of the Equipment Surface 23 6 2 Cleaning and Disinfection of the Cuffs 23 6 3 Cleaning and Disinfection of Cables 23 6 4 Maintenance 24 6 5 Disposal of the Product 24 7 Technical Specifications 25 7...
Страница 5: ...Co KG change order service The revision index a letter that follows the order number changes with every update of the manual Order Number Revision Date Comment A8136 GER Revision A 2018 03 Initial Re...
Страница 6: ...is an integral part of the equipment It will be enclosed in electronic form according to 207 2012 EU The data medium with the electronic manual or the manual in paper form which can be requested free...
Страница 7: ...HYSIO PORT AS A8136 Revision A General Information PAR Medizintechnik GmbH Co KG Sachsendamm 6 10829 Berlin Germany Tel 49 30 235 07 00 Fax 49 30 213 85 42 The country of manufacture is indicated on t...
Страница 8: ...on by professional medical personnel like physicians nurses or medical assistant The Oscillometric Measurement Method The blood pressure is measured by the oscillometric method The criteria for this m...
Страница 9: ...PHYSIO PORT AS Arterial Stiffness can conduct a pulse wave analysis following a non invasive blood pressure measurement If elected the pulse wave analysis is performed right after one of the two bloo...
Страница 10: ...of the proposed combination of equipment The standards IEC 60601 1 or IEC 60950 1 must be observed in any case Connection of this device to an IT network that includes other equipment could result in...
Страница 11: ...the relevant EMC requirements X ray equipment MRI devices radio systems etc are possible sources of interference as they may emit higher levels of electromagnetic radiation Caution Equipment damage ri...
Страница 12: ...recent measurement values or error message Systolic value S diastolic value D and pulse rate HR are displayed successively To mark an event push the info button while the measured values are being dis...
Страница 13: ...YYYY MM format Calibration mark valid in Germany only see Technical Inspection of the Measuring System Symbols used on the display Blinks with each detected oscillation is continuously displayed when...
Страница 14: ...eries is sufficient for up to 48 h of operation or 400 blood pressure measurements The capacity of rechargeable batteries decreases with age If the capacity of fully charged batteries is consider ably...
Страница 15: ...serve the correct polarity when inserting the batteries Note The energy source needs to be selected only when the BP monitor is put into service for the first time or when you change from NiMH to alka...
Страница 16: ...l appear in the charging unit display where each symbol corresponds to one of the charger compartments Fig 3 4 During the charge cycle the corresponding bar in the battery sym bols blinks Note If the...
Страница 17: ...hargeable batteries have a capacity of 100 i e they are fully charged b 50 means that the alkaline batteries have a capacity of only 50 i e they are half depleted The minimum battery capacity for a 24...
Страница 18: ...ause injury to the patient due to blood flow interference The application of the cuff over a wound can cause further injury The application of the cuff and its pressurization on the arm on the side of...
Страница 19: ...ulation of the patient You must hear the connector click into place Ensure that the tube is not kinked or blocked during the measurement To avoid erroneous measurements ensure that the patient does no...
Страница 20: ...ble pouch to remove the pressure hose only in emergency situations see warning below that the cleaning may only be carried out by qualified medical personnel and not by the patient Absolute contraindi...
Страница 21: ...the systolic value of the previous measurement minimum inflation pressure 120 mmHg The determination of the blood pressure values takes place when the cuff pressure is gradually decreased If the measu...
Страница 22: ...r deflation measurement method Tighten the cuff so that one finger but not two can be inserted between the patient s arm and the cuff At the same time the device switches to a deflation rate of 4 mmHg...
Страница 23: ...cessful Incidin Foam or equivalent disinfectants that are used in practices or hospitals are suitable Please respect the information of the manufacturer especially regarding the exposure time After cl...
Страница 24: ...nt please contact PAR Medizintechnik Service for details The nature and extent of the inspections are described in the corresponding sections of the Service Manual Upon request PAR Medizintechnik prov...
Страница 25: ...SIO PORT AS IP02 wearable pouch of the PHYSIO PORT IP22 PHYSIO PORT device in wearable pouch Expected Service Life PHYSIO PORT device 10 years Cuff 20 000 cycles of reapplication 7 1 Blood Pressure Me...
Страница 26: ...flash drive Optional Accessories A2501 Blood pressure cuff for adults small 17 26 cm with D ring A2503 Blood pressure cuff for adults large 32 42 cm with D ring A99042 PHYSIO PORT Manuals USB flash d...
Страница 27: ...eitlinien RF emissions to EN 55011 CISPR 11 Group 1 The PHYSIO PORT devices use RF energy only for their internal function Therefore their RF emissions are very low and are not likely to cause any int...
Страница 28: ...a typical commercial or hospital environment Surge to EN 61000 4 5 IEC 61000 4 5 0 5 kV differential mode 1 0 kV differential mode 0 5 kV common mode 1 0 kV common mode 2 0 kV common mode not applicab...
Страница 29: ...manufacturer and d is the recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electro magnetic site surveya should be less than the compli ance l...
Страница 30: ...ons equipment Rated Maximum Output Power of Transmitter W Separation Distance According to Frequency of Transmitter m 150 kHz to 80 MHz d 1 17 P 80 MHz to 800 MHz d 1 17 P 800 MHz to 2 5 GHz d 2 33 P...
Страница 31: ...t Sometimes the device internally stops the long term measurement In this case deliver the device to the agreed date to your doctor The audio signals of the device are disabled by default If the docto...
Страница 32: ...PAR Medizintechnik GmbH Co KG Sachsendamm 6 10829 Berlin Germany Tel 49 30 2350700 Fax 49 30 2138542 http www par berlin com...
