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Do not proceed until conditions are understood and met.",{"name":70,"@type":61,"acceptedAnswer":71},"Who is allowed to perform repairs or open covers?",{"text":72,"@type":64},"All repairs should be done by personnel authorized by GE Healthcare. 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See definitions below.  \n\n| | WARNING! The WARNING symbol and notice highlight instructions that must be followed to avoid personal injury. Do not proceed until all stated conditions are clearly understood and met. |\n| --- | --- |\n\nCAUTION! The CAUTION notice highlights instructions that must be followed to avoid damage to the product or other equipment. Do not proceed until all stated conditions are met and clearly understood.  \nNotes  \nNote: A Note is used to indicate information that is important for trouble-free and optimal use of the product.  \nRecycling  \nThis symbol indicates that the waste of electrical and electronic equipment must not be disposed as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of equipment.  \n\n| | WARNING! This is a Class A product. In a domestic environment, it might cause radio interference, in which case the user might be required to take appropriate measures. |\n| --- | --- |\n\n\n| | WARNING! All repairs should be done by personnel authorized by GE Healthcare. Do not open any covers or replace parts unless specifically stated in the instructions. |\n| --- | --- |\n\nCE-certification  \nThis product complies with the European directives listed below, by fulfilling corresponding standards. A copy of the Declaration of Conformity is available on request.  \n• 73/23/EEC, Low Voltage Directive  \n• 89/336/EEC, EMC Directive  \nThe CE logo and corresponding declaration of conformity, is valid for the instrument when it is:  \n– used as a stand-alone unit, or  \n– connected to other CE-marked GE Healthcare instruments, or  \n– connected to other products recommended or described in this manual, and  \n– used in the same state as it was delivered from GE Healthcare except for alterations described in this manual.  \nNote: The Declaration of conformity is valid only for  \nsystems that are marked with the CE logo:  \nContents  \nAbout this installation guide .......................................................5  \nSafety ...............................................................................................6  \nPre-requisites .................................................................................9  \nInstallation overview ................................................................. 10  \nInstallation of ÄKTAFPLC ........................................................... 11  \nInstallation test ........................................................................... 16  \nPreparation of ÄKTAF PLC .................................................................................. 16  \nRunning the installation test method .......................................................... 17  \nEvaluating the installation test results ........................................................ 20  \nAutomatic evaluation ................................................................................................... 20  \nManual evaluation ......................................................................................................... 20  \nCorrecting faulty evaluation results ............................................................. 21  \nFaulty gradient ................................................................................................................ 21  \nFaulty step response ..................................................................................................... 22 ","cbCaipsQQnIjbsOH","https://ap.wps.com/l/cbCaipsQQnIjbsOH","pdf",900509,28,"English","# About this installation guide\n## Safety\n## Pre-requisites\n## Installation overview\n## Installation of ÄKTAFPLC\n## Installation test\n## Test record\n## Installation record\n## Registration form\n## Components","[{\"question\":\"What is the intended use of ÄKTAFPLC according to the manual?\",\"answer\":\"ÄKTAFPLC is intended for research use only and must not be used in clinical or in vitro procedures for diagnostic purposes.\"},{\"question\":\"How should warnings and cautions in the manual be handled?\",\"answer\":\"The WARNING symbol highlights instructions to avoid personal injury, while the CAUTION notice highlights instructions to avoid damage to the product or other equipment. Do not proceed until conditions are understood and met.\"},{\"question\":\"Who is allowed to perform repairs or open covers?\",\"answer\":\"All repairs should be done by personnel authorized by GE Healthcare. Do not open covers or replace parts unless specifically stated in the instructions.\"}]","GE Healthcare ÄKTAFPLC - User Manual - Safety Notices | PDF",71]