Huntleigh IRT10 Скачать руководство пользователя страница 16

17

8. Electromagnetic 

Compatibility

Make sure the environment in which the equipment is installed is not subject to strong 
sources of electromagnetic interference (e.g. radio transmitters, mobile phones).

This equipment generates and uses radio frequency energy. If not installed and used 
properly, in strict accordance with the manufacturer’s instructions, it may cause or be 
subject to interference. Type-tested in a fully con

fi

 gured system, complies with EN60601-

1-2, the standard intended to provide reasonable protection against such interference. 
Whether the equipment causes interference may be determined by turning the equipment 
off and on. If it does cause or is affected by interference, one or more of the following 
measures may correct the interference:

 

• 

Reorienting the equipment

 

• 

Relocating the equipment with respect to the source of interference

 

• 

Moving the equipment away from the device with which it is interfering

 

• 

Plugging the equipment into a different outlet so that the devices are  

 

 

 

on different branch circuits

WARNING: The use of accessories, transducers and cables other than 
those speci

fi

 ed, with the exception of transducers and cables sold by the 

manufacturer of the Smartsigns® Compact 300 as replacement parts for 
internal components, may result in increased emissions or decreased 
immunity of the Smartsigns® Compact 300.  

WARNING: The Smartsigns® Compact 300 should not be used adjacent 
to or stacked with other equipment and that if adjacent or stacked use is 
necessary, the Smartsigns® Compact 300 should be observed to verify 
normal operation in the con

fi

 guration in which it will be used 

WARNING:  Portable RF communications equipment (including peripherals 
such as antenna cables and external antennas) should be used no closer 
than 30 cm (12 inches) to any part of the Smartsigns® Compact 300 
including cables speci

fi

 ed by the manufacturer.  Otherwise, degradation of 

the performance of this equipment could result. 

Guidance and Manufacturer’s declaration - electromagnetic emissions

The IRT10 infrared ear thermometer is intended for use in the electromagnetic environment 
speci

fi

 ed below. The customer or the user of the IRT10 infrared ear thermometer should assure that 

it is used in such an environment.

Emissions Test

Compliance

Electromagnetic Environment - guidance

RF emissions
CISPR 11

Group 1

The IRT10 infrared ear thermometer uses RF energy only 
for its internal function. Therefore, its RF emissions are 
very low and are not likely to cause any interference in 
nearby electronic equipment.

RF emissions
CISPR 11

Class A

The IRT10 infrared ear thermometer is suitable for use in 
all establishments, other than domestic and those directly 
connected to the public low-voltage power supply network 
that supplies buildings used for domestic purposes.

Harmonic emissions
IEC 61000-3-2

Class A

Voltage 

fl

 uctuations / 

fl

 icker emissions

IEC 61000-3-3

Complies

Setting up the Monitor

Содержание IRT10

Страница 1: ...Wireless Tympanic Thermometer IRT10...

Страница 2: ...ts 11 4 3 Connecting the Thermometer to the host 11 4 4 Installing the Batteries 12 4 5 Pairing the Thermometer and Main Unit 12 5 Using the Thermometer 13 5 1 Temperature Measurement 13 6 Care Cleani...

Страница 3: ...on History The documentation part number and revision number indicate its current edition The revision number changes when a new edition is printed in accordance with the revision history of the docum...

Страница 4: ...use and ensure its safe and proper use WARNING Before use carefully read directions for use including all warnings cautions and instructions WARNING If the battery shows any signs of damage leakage or...

Страница 5: ...ital Signs Monitor 2 1 Features of the IRT10 Wireless Themometer Physical The IRT10 wireless tympanic thermometer is a clinical grade hand held thermometer indicated for the intermittent measurment of...

Страница 6: ...uld not be used if the following situations are present Do not use the thermometer if there is any blood or drainage in the ear canal Do not use the thermometer if the patient presents with inflamator...

Страница 7: ...trols Indicators Symbols and Displays 3 5 Thermometer Controls and Display 1 2 3 4 5 6 1 Temperature probe status indicator 2 Start measurment 3 Display 4 Infra red sensor 5 Lens ejector 6 Battery com...

Страница 8: ...ption of Symbols Indicators The symbols and Indicators are described as follows Symbols Description Attention consult accompanying documents Battery charging indicator lamp Refer to instructions for u...

Страница 9: ...ormit Europ enne Complies with medical device directive 93 42 EEC Disposal instructions Manufacturer This way Up Fragile Handle with care Limit of stacking layers Keep dry Description of Controls Indi...

Страница 10: ...ing and Inspection The Thermometer is shipped in one carton Examine the carton carefully for evidence of damage Contact Huntleigh Healthcare Ltd Service Department immediately if any damage is discove...

Страница 11: ...y compartment Place new batteries into compartment paying attention to the polarity close the compartment ensuring it snaps into place The system is ready for use 4 5 Pairing the Thermometer and Main...

Страница 12: ...ens cover in accordance with the local regulations During the monitoring process the temperature measuring instrument will automatically check itself once per hour Self checking will last 2 seconds an...

Страница 13: ...hat the measurement is complete 5 Remove the thermometer 6 The measurement will be shown on the thermometer s screen it will be automatically transferred to the monitor Thermometer display Monitor dis...

Страница 14: ...n is not available use a suitable carton with appropriate packing material to protect the device during shipping Return by any shipping method that provides proof of delivery 6 3 Service Apart from a...

Страница 15: ...f range 10 40 C 33 8 39 2 F Move the device to appropriate environment and wait 30 minutes prior to taking a temperature Er2 The environment temperature is not stable Do not take measurement until the...

Страница 16: ...The Smartsigns Compact 300 should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary the Smartsigns Compact 300 should be observed to verify norm...

Страница 17: ...may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people a The ISM industrial scientific and medical bands between 150 k...

Страница 18: ...e s 2 kV line s to earth Mains power quality should be that of a typical commercial or hospital environment Voltage dips short interruptions and voltage variations on power supply input lines IEC 6100...

Страница 19: ...power of transmitter W Separation distance according to frequency of transmitter m 150kHz to 80MHz d 1 2 P 80MHz to 800MHz d 1 2 P 800MHz to 2 5GHz d 2 3 P 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 1...

Страница 20: ...AMMABLE ANAESTHETIC MIXTURE WITH AIR OXYGEN OR NITROUS OXIDE 9 2 Standards MDD 93 42 EEC EN ISO13485 2012 AC2012 EN ISO14971 2012 EN 60601 1 2006 AC 2013 EN 60601 1 2 2007 AC 2010 EN60601 1 6 2010 EN...

Страница 21: ...700 hPa to 1060 hPa Note The system may not meet its performance specifications if stored or used outside the manufacturer s specified temperature and humidity range 9 5 Measurement Parameters Probe T...

Страница 22: ...aned to the outside of the package Mark the package Service Department For further details refer to NHS document HSG 93 26 UK only Huntleigh Diagnostics reserve the right to return product that does n...

Страница 23: ...rjoHuntleigh House Houghton Hall Business Park Houghton Regis Bedfordshire LU5 5XF Registered No 942245 England Wales Registered Office Huntleigh Healthcare Limited 2017 As our policy is one of contin...

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