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#Icad digitizer manual
The following symbol indicates the operator should consult the manual for additional information. Correct and safe operation of the digitizer requires familiarity with information that is not marked on the product.
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Power cords used with this device in Europe must meet the requirements of IEC 227 Designation 53 or IEC 245 Designation 53. Power cords used with this device in North America must be rated by Underwriters Laboratories for hospital use.
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This product provides Class I medical device protection against electrical shock. This product is not suitable for use in the presence of flammable anesthetic mixtures with air or with oxygen or with nitrous oxide. It provides no protection against the ingress of water. This product is in the Ordinary Equipment Class. To maintain Medical Equipment Certification, the digitizer must be connected to a host computer that has been configured in accordance with IEC 6. This product is intended to be turned on and left on. This product’s function and intended use is making digital copies of medical x-ray films. 601.1ĥRA9 DiagnosticPRO® Advantage, DosimetryPRO® Advantage and CADPRO® Advantage carry the CE mark, issued by BSI. Safety and compliance information MEDICAL EQUIPMENT WITH RESPECT TO ELECTRIC SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH UL60601-1, IEC60601-1 AND CAN/CSA C22.2 No. Voltage: 100 to 240 VAC Current: 0.75 to 1.5 A Frequency: 47 to 63 Hz Temperature: 10☌ to 30☌ (60☏ to 85☏) Relative humidity: 20% to 85%, non-condensing Atmospheric pressure: 696 to 1013hPa (10,000 to 0 ft) Modifications to the digitizer or the VIDAR shielded cables or the use of cables other than those available from VIDAR could void the user’s authority to operate the equipment. Product compliance testing was conducted using VIDAR shielded cables. Operation of this equipment in a residential area can cause harmful interference, in which case the user will be required to correct the interference at his or her own expense. This equipment generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with the instruction manual, may cause harmful interference to radio communications. These limits are designed to provide reasonable protection against harmful interference when the equipment is operated in a commercial environment. Radio Frequency Emissions This equipment has been tested and found to comply with the limits for a Class A digital device, pursuant to Part 15 of the FCC Rules. Atencion: Acceso interno solo autorizado a personal tecnico cualificado. Toute operation de maintenance doit etre effectuee par une personne qualiee. Attention: Aucune piece ne peut etre remplacee par l’utilisateur. Wartung uno reparatur nur durch eletrofachkräfte. Phone: 1-70 Fax: 1-70 Internet: Technical Support: Phone: 1-800-471-SCAN or 1-70 E-mail: Įmergo Europe Molenstraat15 2513 BH, The Hague The Netherlands
#Icad digitizer software
The software developer is ultimately responsible for detailing the Contraindications for the PACS System (or Teleradiology software package) or Oncology Systems as a whole, including the digitizer.ģ65 Herndon Parkway Herndon, VA 20170 U.S.A. The digitizers are marketed as a component to application software development companies, who will incorporate the digitizer into their respective PACS or Teleradiology, CAD system(s). These third-party software packages or complete systems are approved separately from a regulatory perspective.
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The manufacturer of the application software will determine specific indications for use. NOTE The digitizers do not include application specific software (Picture Archiving and Communications system, Teleradiology, Oncology Systems, or Computer Aided Detection software). Terms denoted by the trademark symbol (™ or ®) used in this publication are trademarks or service marks registered in the United States or other countries. © Copyright 2010 by VIDAR® Systems Corporation.