KaVo EXPERTsurg LUX 1.008.3500 Instructions For Use Manual

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KaVo EXPERTsurg LUX 1.008.3500 Instructions For Use Manual Manual pdf 11 page image

Instructions for use EXPERTsurg LUX REF 1.008.35002 Safety | 2.3 Disposal of electronic and electrical devicesNoteKaVo cannot guarantee the compliance of accessories, cables, and other compon-ents not supplied by KaVo with the EMC requirements of IEC 60601-1-2 (DIN EN60601-1-2).2.3 Disposal of electronic and electrical devicesNoteAccording to EC directive 2012/19 concerning used electrical and electronicdevices, this product is subject to the cited directive and must be disposed of ac-cordingly within Europe.For more information, please visit www.kavo.com or contact your specialised dentalsupplier.For final disposal:In GermanyTo return an electrical device, you need to proceed as follows:1. On the homepage www.enretec.de of enretec GmbH, you can download a form fora disposal order under the menu item eom. Download the disposal order or com-plete it as an online order.2. Enter the corresponding information to complete the order, and submit it as an on-line order or by fax +49 (0)3304 3919 590 to enretec GmbH.The following contact options are also available for questions and for initiating adisposal order:Phone: +49 (0) 3304 3919-500Email: eom@enretec.de andPostal address: enretec GmbH, Geschäftsbereich eomRECYCLING®Kanalstraße 17D-16727 Velten3. A unit that is not permanently installed will be picked up at the office.A permanently installed unit will be picked up at the curb at your address on theagreed date.The owner or user of the device will have to bear the cost of disassembly, trans-portation and packaging.InternationalFor country-specific information on disposal, contact your dental supplier.2.4 Safety instructionsWARNINGApplication of un-authorised accessories or un-authorised modifications of theproduct.Accessories that have not been approved and/or inadmissible modifications of theproduct could lead to hazards and/or personal injury or property damage.▶ Only use accessories that have been approved for combination with the productby the manufacturer or are equipped with standardised interfaces (e. g. MULTIflexcouplings, INTRAmatic).▶ Do not make any modifications to the device unless these have been approved bythe manufacturer of the product.11 / 72