Samsung Accuvix A30 v3.00.00 Vol1 E free download

File name Accuvix_A30_v3.00.00_Vol1_E.pdf

Volume 1 Diagnostic Ultrasound System Operation Manual Version 3.00 English MI68-02890A PROPRIETRAY INFORMATION AND SOFTWARE LICENSE The Customer shall keep confidential all proprietary information furnished or disclosed to the Customer by Samsung Medison unless such information has become part of the public domain through no fault of the Customer. The Customer shall not use such proprietary information, without the prior written consent of Samsung Medison, for any purpose other than the maintenance, repair or operation of the goods. Samsung Medison systems contain Samsung Medison proprietary software in machine-readable form. Samsung Medison retains all its rights, title and interest in the software except that purchase of this product includes a license to use the machine-readable software contained in it. The Customer shall not copy, trace, disassemble or modify the software. Transfer of this product by the Customer shall constitute a transfer of this license that shall not be otherwise transferable. Upon cancellation or termination of this contract or return of the goods for reasons other than repair or modification, the Customer shall return to Samsung Medison all such proprietary information. Safety Requirements Classifications: X of protection against electrical shock: Class I Type XDegree of protection against electrical shock (Patient connection): Type BF or CF Applied Part XDegree of protection against harmful ingress of water: Ordinary equipment XDegree of safety of application in the presence of a flammable anesthetic material with air or with oxygen or nitrous oxide: Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide. XMode of operation: Continuous operation Electromechanical safety standards met: XMedical Electrical Equipment, Part 1: General Requirements for Basic Safety and Essential Performance [IEC 60601-1:2005/A1:2012] XMedical Electrical Equipment, Part 1-2: General Requirements for Basic Safety and Essential Performance- Collateral Standard: Electromagnetic Compatibility - Requirements and Tests [IEC 60601-1-2:2007] XMedical Electrical Equipment, Part 1-6: General Requirements for Basic Safety and Essential Performance- Collateral Standard: Usability [IEC 60601-1-6:2010] XMedical Electrical Equipment, Part 2-37: Particular Requirements for the Basic Safety and Essential Performance of Ultrasonic Medical Diagnostic and Monitoring Equipment [IEC 60601-2-37:2007] XMedical Electrical Equipment, Part 1: General Requirements for Safety [IEC 60601-1:1988 with A1:1991 and A2:1995] XMedical Electrical Equipment, Part 1-1: General Requirements for Safety - Collateral Standard: Safety Requirement for Medical Electrical Systems [IEC 60601-1-1:2000] XMedical Electrical Equipment, Part 1-2: General Requirements for Safety - Collater