Buck LED VISION (K) Instruction Manual

Light source

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Light source
[K]
LED VISION
Instruction manual
LED Light source for endoscopic applications
1

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Summary of Contents for Buck LED VISION (K)

  • Page 1 Light source LED VISION Instruction manual LED Light source for endoscopic applications...
  • Page 2 Manufacturer: Distributor: ILO electronic GmbH EMOS Technology GmbH Carl-Zeiss-Str. 3 Gewerbestr. 10 25451 Quickborn / Germany 88636 Illmensee / Germany Phone: +49 (0) 4106-7758-0 Phone: +49 (0) 7558/ 938 278 – 0 Fax: + 49 (0) 7558/ 938 278 – 55 www.ilo.com info@ilo.com www.emostechnology.com...
  • Page 3 Index General Information �������������������������������������������������������������������������������������������������������������������������������������������������������� 4 Data of the Device ................................... 4 Warranty ....................................4 Services, Repairs, Modifications ............................. 4 Responsibility ..................................4 Reporting requirement ................................4 Rights ....................................... 4 Disposal ....................................4 Safety reference / Place the equipment ��������������������������������������������������������������������������������������������������������������������������� 5 Intended use ...................................
  • Page 4: General Information

    General Information Thank you for purchasing a product from our company and therefore have placed your trust in a modern and high-quality device. Our name stands for long years of experience and diligence in the development and production of light sources and camera systems.
  • Page 5 Safety reference / Place the equipment Intended purpose / intended use The device described in these instructions serves as a basic device for generating/providing light to illuminate the surgical site (surgical field) during minimally invasive surgical procedures (endoscopy). Only use the device with accessories, consumables and disposable items that are marked as accessories by the manufac- turer or whose safety-related and biologically harmless usability has been proven.
  • Page 6: Description Of The Unit

    • The device must not be operated near flammable gases or flammable substances, and within the direct patient environ- ment. • Connectors of fiber optics and the lamp unit might be hot. Please observe a cooling time of 15 minutes before changing or replacing parts.
  • Page 7: Installation And Activation

    Installation and activation Receiving inspection The device and the delivered accessories have to be examined for completeness and apparent damages on receipt. To as- sert your rights, transport damages must be reported immediately (within 24 hours) to the deliverer. Please always use the original packing if you return the device and the additional instruments.
  • Page 8: Connectivity Options

    Connectivity options...
  • Page 9: Control Elements / Connections

    Control elements / Connections Front view Note labeling style for the front view: „ “ Rear view Note labeling style for the front view: „ “...
  • Page 10 Description of the control elements and connections This connector is used to connect the fibre optics to the light source. The light source is Connector fibre optics: delivered as standard with STORZ adaptor and optional with TURRET adaptor. You can con- nect light guides of different makes to the TURRET adaptor Attention! Using the wrong light guide or adaptor can damage the light source and the accessories and threats the patient.
  • Page 11 Basically, the control unit is protectively earthed by the 3-pin power supply cord when it is Equipotential terminal connect to a protectively earthed wall socket, as prescribed. When running the equipment in rooms which comply to group 2 acc. DIN VDE 0100, the control unit must be joined to the central potential equalisation of the operating theatre or of the equipment trolley by means of a grounding cable.
  • Page 12 Operating Power-up Before connecting a light cable into a light source adapter of the equipment, please ensure that you have the correct plug and adapter. A plug that is too long or too thin can for example be pushed too far into the equipment, and can damage the sensitive diaphragm or lens inside.
  • Page 13 Notice and warning messages The error codes are displayed at the „Intensity“ bar graph . During operation, the display changes in 1 sec. / 2 sec. inter- vals between the display of the light intensity and the error codes. The error code is received after switching off (standby mode).
  • Page 14: Service Interval

    Service instructions General maintenance and repair instructions The information contained in this chapter is only intended for properly trained personnel, which is proficient in the required knowledge and security arrangements for the repair of electronic equipment. The manufacturer assumes no li- ability for repairs and modifications carried out by unauthorized personnel.
  • Page 15: Troubleshooting

    Cleaning / Desinfection Attention! Disconnect the main power plug prior to beginning the cleaning / disinfection! All external surfaces of the device are resistant to all common cleaners and disinfectants, so that these may be used without restrictions. For the application of cleaning and disinfecting liquids, a soft cloth or blotting paper should be used to avoid scratching the surface and to better dispense and distribute the liquid.
  • Page 16: Specifications

    Specifications Technical Data General data Mains voltage: 100-240 VAC Power consumption: 130 VA Mains fuses: Fine fuses, 5x20mm, delay acting 3,15A / 250V with high breaking capacity (Ia = 1500 A) Dimensions (WxHxD): Device: 360 x 125 x 351 mm LED module: ·...
  • Page 17: Electromagnetic Compatibility

    Annex Electromagnetic compatibility • The present device corresponds to the following standard: IEC 60601-1-2 • Precautionary measures Electro-medical devices are subject to special precautionary measures concerning electromagnetic compatibility (EMC). This device is to be used for the purposes described in the operation manual and has to be installed, set up, and operated in com- pliance with the EMC guidelines.
  • Page 18 • Manufacturer’s declaration – Electromagnetic immunity: Ful- Immunity tests Test level Electromagnetic environment – Guidelines filled Electrostatic discharge (ESD) ± 2; 4; 6; 8 kV Floors should be made of concrete or wood according to IEC 61000-4-2 or covered with ceramic tile. If the floor is Contact discharge covered with synthetic material and offers no ESD protection, the relative humidity...
  • Page 19 Fast transient electrical dis- ± 2 kV 100 kHz supply lines turbances/bursts according to ± 1 kV 100 kHz signal and data IEC 61000-4-4 lines Surges according to IEC ± 0,5 kV, ± 1 kV 100 kHz (line 61000-4-5 to line) ±...
  • Page 20: Maintenance Report

    Maintenance report User Address Serial-No.: Servicing check up Name Date Signature...
  • Page 21 Icons (Instruction manual) Attention, important information! Service information Symbols (Medical device) Follow instructions for use (EN ISO 7010-M002) Follow instructions for use (EN ISO 15223-1, 5.4.2) Application part type: BF (IEC 60417-5333) - Connection Connection for potential equalization (IEC 60417-5021) - Connection Grounding (IEC 60417-5021) Corresponds to the EU regulation 2017/745, annex V Do not dispose of with household waste (ElektroG / WEEE 2012/19/EU)
  • Page 24 ILO electronic GmbH Carl-Zeiss-Str. 3 25451 Quickborn / Germany Phone: +49 (0) 4106-7758-0 www.ilo.com info@ilo.com...

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