TIM ARKON Instructions For Use Manual Download Page 10

2 Safety information  

10 

ARKON Data Bridge, SW 1.00.n, Instructions for Use (en-GB) 

2.1.7 

 Delays in transmission 

 
Signals of measurements and alarms from the MIRUS Controller may be delayed before being 
transferred to a patient monitor. This delay time may vary depending on the conditions in which the 
Data Bridge is working. For this reason, specified delay times cannot be provided. 

   Only use the MIRUS Controller as the primary source for alarms and for viewing 

measurements. 

   Refer to the manufacturer's instructions regarding patient monitor delay times. 

 
 
 

2.1.8 

Deviations in transmission 

 
The data transferred to a patient monitor may be displayed incompletely or incorrectly on the 
monitor.  
 

Alarms 

The various alarm priorities may be displayed differently on the patient monitor than on the MIRUS 
Controller connected via the Data Bridge. 

   Check which alarms are assigned to which alarm priorities. 

   Only use the MIRUS Controller alarm system as the primary alarm source. 

 
 

Measurements 

In certain cases, there may be differences between the measurements displayed on the patient 
monitor and the measurements displayed on the MIRUS Controller connected via the Data Bridge. 

   Only use the MIRUS Controller as the primary source for viewing measurements. 

 
 
 

2.1.9 

Modifications to the device 

 
Modifications to this device may lead to malfunctions and unforeseeable hazards, possibly causing 
personal injury or damage to property. 

   Do not modify this device. 

 
 
 

2.1.10  Accessories 

 
The Data Bridge has been tested for electromagnetic compatibility with the accessories on the 
accessories list. The Data Bridge's electromagnetic emissions may be increased, and the 
interference immunity may be reduced, if accessories not included on the accessories list are used. 
Moreover, the proper functioning of the Data Bridge may be affected, possibly resulting in personal 
injury or damage to property. 

  Only use the accessories specified by the manufacturer. 

  Other accessories may only be used if they do not affect the electromagnetic compatibility. 

 

Summary of Contents for ARKON

Page 1: ...Instructions for Use ARKON Data Bridge Philips Option SW 1 00 00...

Page 2: ......

Page 3: ...ARKON Data Bridge SW 1 00 n Instructions for Use en GB 3 Page intentionally left blank...

Page 4: ...Numerals in illustrations represent elements that are referred to in the text A Consecutive letters represent actions A new sequence of actions starts again from A The triangle represents the outcome...

Page 5: ...smission 10 2 1 8 Deviations in transmission 10 2 1 9 Modifications to the device 10 2 1 10 Accessories 10 2 1 11 Electromagnetic compatibility EMC 11 2 1 12 Infection risk 11 2 2 Warnings in these In...

Page 6: ...0 Table of contents 6 ARKON Data Bridge SW 1 00 n Instructions for Use en GB 12 Technical data 29...

Page 7: ...ied and the following functions are supported Display of parameter data etCO2 and etVA Signalling of certain high priority alarms Transfer of device settings MACset 1 2 Operator and user qualification...

Page 8: ...Use in an accessible place 2 1 2 Symbols and product labels If symbols and product labels are not observed it may result in personal injury or damage to property Observe symbols and product labels 2...

Page 9: ...nal injury or damage to property Only operate the Data Bridge with the original mains adapter Ensure that the protective earthing of the electrical installation is working properly 2 1 6 Connected dev...

Page 10: ...MIRUS Controller alarm system as the primary alarm source Measurements In certain cases there may be differences between the measurements displayed on the patient monitor and the measurements display...

Page 11: ...antistatic gloves Comply with the requirements for the electromagnetic environment Only use approved electronic accessories e g mains adapter Electromagnetic disturbances If devices that emit electro...

Page 12: ...mation about a possible hazard and instructions on how to avoid the hazard They are divided into different hazard levels depending on the degree of the danger WARNING Denotes a hazard with a medium de...

Page 13: ...FireWire connector 1 b for connecting the ARKON Data Bridge to the MIRUS Controller Connecting cable 2 with USB 2 0 connector 2 a and RS232 connector 2 b for connecting the ARKON Data Bridge to the p...

Page 14: ...cription 1 LED display yellow Data communication 2 LED display green Mains power supply 3 USB 1 USB interface for connecting the MIRUS Controller 4 USB 2 USB interface for connecting the IntelliBridge...

Page 15: ...waste Follow the Instructions for Use Warning Alerts the user to refer to the Instructions for Use for important safety information such as warnings and precautions Regulation 2014 30 EU Serial numbe...

Page 16: ...lliBridge EC5 ID module open interface Philips article number 865114 option 101 When connecting to patient monitor MX400 450 integrated IntelliBridge EC10 interface Philips article number 866060 86606...

Page 17: ...ct the MIRUS Controller to the mains power supply C Plug the USB connector 2 a of the connecting cable 2 into the USB port 2 on the device D Plug the RS232 male connector of the IntelliBridge EC5 ID m...

Page 18: ...he power supply using the mains adapter supplied On the ARKON Data Bridge the green LED for the mains power supply is illuminated I The patient monitor set up occurs automatically after the data commu...

Page 19: ...ontroller 5 1 Measurements Measurements Description Unit etDES End tidal concentration of the volatile anaesthetic v v etISO etSEVO etCO2 End tidal concentration of CO2 mmHg 5 2 Settings on the MIRUS...

Page 20: ...ration was exceeded 11 13 ETCO2 LOW The lower alarm limit for the etCO2 concentration was exceeded 12 ETCO2 HIGH The upper alarm limit for the etCO2 concentration was exceeded Technical alarms ID of t...

Page 21: ...ions for Use en GB 21 ID of the alarm notification originating from the MIRUS Controller Display of the alarm notification on the patient monitor Condition 25 26 27 29 30 31 DEVICE FAILURE A technical...

Page 22: ...shed because the device is not connected to the MIRUS Controller or the patient monitor Connect device to the MIRUS Controller Connect device to the EC10 interface on the patient monitor or the Intell...

Page 23: ...ce disinfectants listed in the following table are suitable for wipe disinfection These disinfectants have been tested by the device manufacturer and they demonstrated material compatibility at the ti...

Page 24: ...r Use en GB Procedure A Disconnect the device from the power supply B Remove all other connecting cables C Carry out wipe disinfection D Remove any remaining disinfectant after the exposure time E Let...

Page 25: ...These consist of inspection assessment of the current condition of the device replacement of wearing parts and checking the functioning of individual device components Repair Corrective measures to re...

Page 26: ...device in accordance with statutory regulations For countries covered by the EU Directive 2012 19 EU This device falls within the scope of the EU Directive 2012 19 EU WEEE on waste electrical and ele...

Page 27: ...g the device The device can be sent to a manufacturer authorized service organisation or the manufacturer for repair or disposal at the end of its service life WARNING Risk of infection The device may...

Page 28: ...ector FireWire connector MC SC DC 01 Connecting cable 2 USB 2 0 connector RS232 female connector AR PH 002 Mains adapter including power cable USB micro USB AR PS 001 ARKON Basic Unit AR PH 003 ARKON...

Page 29: ...nal voltage Current 5V direct current 2 5 A max Electromagnetic compatibility pursuant to EN 60601 1 2 Test parameters and threshold values may be obtained from the manufacturer if required Compatible...

Page 30: ...Notes 30 ARKON Data Bridge SW 1 00 n Instructions for Use en GB...

Page 31: ......

Page 32: ...30 56070 Koblenz Germany Germany Tel 49 261 899 689 00 Fax 49 261 899 689 09 info tim gmbh de http www tim gmbh de This document ARKON Data Bridge Philips Option Instructions for Use en GB Ident no 06...

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