Ackerman 16-2028 Скачать руководство пользователя страница 5

USER MANUAL 16-2028 

Rev. 04/2017

• Do not expose the device to an excessively humid environment or where it could be sprayed with water.

• Only use the accessories supplied with the device or optional accessories recommended by the
manufacturer.

• Do not place any heavy objects on the device.

• This device is not sterile.

• If the power cord is damaged, immediately switch off the device. It is dangerous to operate this device
with a damaged cord.

• To disconnect the cord, pull out the plug. Never pull on the cord itself.

• Disconnect the device from the mains if you do not expect to use it for a few days or longer.

• Ensure there is sufficient air circulating to prevent overheating inside the device: at least 15 cm all
around the device. Do not cover the device and make sure the feet of the device are present.

• Do not use corrosive or abrasive products to clean the device, but only use the disinfectant liquids
recommended in section 8.

• Before using the device, make sure it does not have any rough surface, sharp edges or protuberances
that might cause safety problems.

• The surface temperature can reach 41°C (after a few minutes’ use). Therefore avoid keeping this area
in contact with the patient.

• To avoid any risk of electric shock, this device should only be connected to an earthed power supply.

• This device must not be modified without the manufacturer’s authorisation. If the medical device is
modified, an inspection and test must be performed to ensure the medical device complies with the
safety instructions.

• Before use, check with the manufacturer that your endoscope is compatible with this device.

• This device must be used on individuals (patients) capable of undergoing an endoscopic procedure.

• Never look directly at the light aperture or the end of the light cable.

• Do not insert anything other than a light cable into the housing [C1] as this may damage the optical
system.

• The use of cables or accessories other than those specified may result in increased emissions or
decreased immunity of the device.

• After use of the source, when the fibre is being withdrawn from its light guide, the temperature on the
metal coupling of the fibre is very high and can cause burns.

• The light power at the fibre outlet can cause eye damage. Take care when handling the fibre while the
device is in use.

• Do not place the distal end of the light cable or the endoscope directly on the patient or any other
inflammable material (surgical drapes, gauze, etc.) because it may be very hot and may cause burns.

It is advisable to have a second light source available in the operating theatre, which can be used

            as a replacement if performance is seen to be reduced or absent.

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Содержание 16-2028

Страница 1: ...USER MANUAL 16 2028 LED LIGHTSOURCE ...

Страница 2: ...manufacturer The manufacturer will appreciate any errors or anything unclear in this operating manual being pointed out to us by users of our products Due to the continuing progress and development of our products we reserve all rights for technical alterations Rev 04 2017 SERVICE ADDRESS Ackermann Instrumente GmbH Eisenbahnstrasse 65 67 78604 Rietheim Weilheim Germany Tel 49 0 7461 96617 0 Fax 49...

Страница 3: ...STANDARDS AND REGULATIONS 5 5 INSTALLATION OF THE LIGHTSOURCE 6 6 OPERATION 7 7 DESCRIPTION OF BACK PANEL 7 8 RECOMMENDED DECONTAMINATION PROCEDURE 8 9 AFTER SALES SERVICE AND MAINTANCE 10 10 TROUBLESHOOTING 12 11 TECHNICAL SPECIFICATIONS 13 12 ELECTROMAGNETIC COMPATIBILITY 13 13 SYMBOLS 14 PAGE 3 OF 14 ...

Страница 4: ...lumination power and precise manual adjustment of light intensity make this the perfect multidisciplinary medical instrument This device comprises A power cord A user manual A quick start guide Optional accessories Universal light cable Adapters for universal light cable source side Storz and Olympus and endoscope side Storz Olympus Wolf S N ACMI Stryker We advise selecting the following diameter ...

Страница 5: ...vice should only be connected to an earthed power supply This device must not be modified without the manufacturer s authorisation If the medical device is modified an inspection and test must be performed to ensure the medical device complies with the safety instructions Before use check with the manufacturer that your endoscope is compatible with this device This device must be used on individua...

Страница 6: ...turer s contact details please refer to the last page of the manual 4 4 END OF LIFE This appliance is marked according to the European Directive 2002 96 EEC on Waste Electrical and Electronic Equipment WEEE By ensuring this product is disposed of correctly you will help prevent potential negative consequences for environment and human health which could otherwise be caused by inappropriate waste h...

Страница 7: ...e light cable a logo indicating the iris mode will be displayed on the screen L2 Pressing or turning the adjustment knob S2 enables the user to exit this mode and to release the light A bar graph indiquates the level of intensity will then appear L2 Turning the adjustment knob S2 clockwise will increase the light intensity and turning it anti clockwise will reduce the intensity An empty bar graph ...

Страница 8: ...hods and or tools are chosen it remains the sole responsibility of the personnel involved This device is not autoclavable The existing alkaline solutions for disinfection of certain medical devices are PROHIBITED for disinfecting this device 9 AFTER SALES AND MAINTANCE No special maintenance is required for this device Note incorrect or faulty use is not covered by the guarantee If a problem persi...

Страница 9: ...position and it can be re used Check that there is enough space around the source to ensure adequate cooling 15 cm all around the device Check that nothing is obstructing the air vents on the back and underneath the source The light source is in iris mode Press the adjustment knob S2 or turn it in order to release the light If the fault persists and the device needs to be returned to our After Sal...

Страница 10: ...xygen or nitrous oxide Standards Electrical safety class 1 type CF Complies with the European Directive 93 42 EEC Class I Complies with the international standards IEC 60601 1 IEC 601 2 18 IEC 60417 and EN 980 This product is fitted with group 1 LEDs in accordance with the standard IEC 62471 Do not look directly into the light to avoid any risk of eye damage 12 ELECTROMAGNETIC COMPATIBILITY 12 1 G...

Страница 11: ...USER MANUAL 16 2028 Rev 04 2017 12 2 GUIDE AND DECLARATION OF THE MANUFACTURER ELECTROMAGNETIC IMMUNITY PAGE 11 OF 14 ...

Страница 12: ...USER MANUAL 16 2028 Rev 04 2017 12 3 GUIDE AND DECLARATION OF THE MANUFACTURER ELECTROMAGNETIC EMISSIONS PAGE 12 OF 14 ...

Страница 13: ...USER MANUAL 16 2028 Rev 04 2017 12 4 RECOMMENDED SEPARATION DISTANCES BETWEEN PORTABLE AND MOBILE RF COMMUNICATION SYSTEMS AND THIS PRODUCT PAGE 13 OF 14 ...

Страница 14: ...USER MANUAL 16 2028 Rev 04 2017 13 SYMBOLS PAGE 14 OF 14 ...

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