Carestream Health RVG00002 WiFi and RFID Control Box User Manual SM737 RegulatoryGd

Carestream Health, Inc. WiFi and RFID Control Box SM737 RegulatoryGd

Contents

Manual - Regulatory

KODAK RVG 6500 System and KODAK RVG 6500 IPS SystemSafety, Regulatory & Technical Specification User Guide
NoticeThe Regulatory Information & Technical Specifications User Guide for the KODAK RVG 6500 System and KODAK RVG 6500 IPS System includes information on the safety instructions, regulatory information and the technical specifications of the device. We recommend that you thoroughly familiarize yourself with this Guide in order to make the most effective use of your system.The information contained in this Guide may be subject to modification without notice, justification or notification to the persons concerned.No part of this Guide may be reproduced without the express permission of Carestream Health, Inc.U.S. Federal law restricts this device to sale by or on the order of a dentist or physician.This document is originally written in English.Manual Name: KODAK RVG 6500 System and KODAK RVG 6500 IPS System Safety, Regulatory and Technical Specifications User GuidePart Number: SM737Revision Number: 02Print Date: 06/2010The Brand names and logos reproduced in this Guide are copyrightKODAK is a trademark of KODAK used under Licence.KODAK RVG 6500 System, complies with Directive 93/42/CEE relating to medical equipment.ManufacturerAuthorized Representative in the European CommunityTROPHY 4, Rue F. Pelloutier, Croissy-Beaubourg77435 Marne la Vallée Cedex 2, France0086Carestream Health, Inc.150 Verona StreetRochester NY 14 608EC REP
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed02 iiiContentsChapter 1Safety InformationIndications for Use   .  .  .   .  .  .   .  .  1Conventions in this Guide  .  .  .   .  .  1Warning and Safety Instructions  .  .  2Hygiene and Disinfection   .  .  .   .  .  5Marking and Labeling Symbols    .  .  6Label Locations .  .   .  .  .   .  .  .   .  .  7KODAK RVG 6500 With or Without IPS System Battery Specification  .  8Chapter 2Regulatory InformationGeneral Regulatory Information   .  .  9Compliance with International Regulations .   .  .  .   .  .  .   .  .  .   .  .16FCC Requirements for USA .  .   .  .16IC Requirements for Canada.  .   .  .17Declaration of Conformity with the R-TTE Directives   .   .  .  .   .  .  .   .  .18Chapter 3Technic al SpecificationsFactory  .  .  .   .  .  .   .  .  .   .  .  .   .  .19Manufacturer:  .  .  .   .  .  .   .  .  .   .  .19Model.   .  .  .   .  .  .   .  .  .   .  .  .   .  .19KODAK RVG 6500 With or Without IPS System Technical Specifications .  .  .   .  .  .   .  .  .   .  .19Minimum Computer System Requirement   .  .  .   .  .  .   .  .  .   .  .21RFID Technical Specification   .   .  .22WiFi Network Technical Specification   .  .  .   .  .  .   .  .  .   .  .22KODAK RVG 6500 With or Without IPS System Environmental Requirements .  .  .   .  .  .   .  .  .   .  .23
iv
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed02 11 Safety InformationIndications for UseThe KODAK RVG 6500 System, wireless digital intra-oral X-ray system, is intended to produce an image of the dental area at the direction of health care professionals of dento- maxillo-facial region of the human anatomy.The KODAK RVG 6500 IPS System, in addition, provides the Intelligent Positioning System to enable the dentist prior to acquisition to correctly align the X-ray beam to the RVG sensor.Conventions in this GuideThe KODAK RVG 6500 Systems is composed of the KODAK RVG 6500 System and the KODAK RVG 6500 Intelligent Positioning System (IPS) System. The following special messages emphasize information or indicate potential risk to personnel or equipment.WARNING:  Warns you to avoid injury to yourself or others by following the safety instructions precisely.Important:  Alerts you to a condition that might cause problems.Tip: Provides extra information and hints.
2 Chapter 1  Safety InformationWarning and Safety InstructionsWARNINGSDevice:•Read and understand this Safety Information before using the KODAK RVG 6500 with or without IPS System.•This device complies with FCC and Industry Canada RF radiation exposure limits set forth for general population (uncontrolled exposure). This device must be installed to provide a separation distance of at least 20cm from all persons and must not be collocated or operating in conjunction with any other antenna or transmitter.•You are responsible for the operation and maintenance of this device. Only legally qualified persons can operate this device. When necessary, have a trained authorized service technician carry out inspection and maintenance operations. •Install this device in an X-ray room that complies with current installation standards. From this location, you must be able to maintain visual or audio communication with the patient and be able to access the Acquisition interface module during exposure. •DO NOT operate the device if there is the threat of an earthquake. Following an earthquake, ensure that the device is operating satisfactorily before using it again. Failure to observe this precaution may expose patients to hazards.•X-ray equipment is hazardous to patients and the operator if you do not observe the exposure safety factors and operating instructions.•DO NOT place objects within the field of operation of the device.•Connect this equipment ONLY to a mains power supply with protective ground to avoid any risk of electric shock.•To dispose of the device or its components, contact a service technician.•No modification of this equipment is allowed.Note:  Emphasizes important information.
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed02 3•DO NOT use this device in conjunction with oxygen-rich environments. This device is not intended for use with flammable anesthetics or flammable agents.•Using accessories other than those specified in this document with the exception of those sold by Carestream Health may result in a lower level of security for the entire system.
4 Chapter 1  Safety InformationComputer:•DO NOT place the computer and the peripheral equipment connected to it in the immediate vicinity of the patient in the unit. Leave at least 1.5 m distance between the patient and the unit. The computer and the peripheral equipment must conform to the IEC60950 standard.•See your computer installation guide for details of the data processing system and screen. Leave a sufficient amount of clear space around the CPU to ensure that it is properly ventilated.•To obtain maximum image quality and visual comfort, position the screen to avoid direct light reflections from internal or external lighting.•The computer and its screen should ideally be situated in or close to the operating area, in the visual field of the practitioner when he is with the patient. The visual access of the acquired image for the patient encourages communication.•The KODAK RVG 6500 systems must run on a computer with a keyboard.•The KODAK RVG 6500 systems must run on a computer with a mouse equipped with a right and left button and a mouse wheel.Control Box and IPS Battery:•To assure proper operation, use only the KODAK RVG 6500 System battery.•Keep the battery out of the reach of children.•Do not leave the battery without surveillance it could be swallowed by a child or animal. In this case call urgently the doctor.•Damaged or oxidized battery can burn the skin if in contact with the skin.•Do not heat nor dispose of the battery in the fire. It can burst or release toxic chemicals.•Do not short circuit the battery.•Do not disassemble, apply excessive pressure or deform the battery.•Avoid placing the battery in reverse polarity.•Battery disposable method must be in accordance with local and state regulations.•Remove the batteries if not used for a long period of time.
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed02 5Hygiene and DisinfectionWARNINGS•Never place the sensor and/or control box in an autoclave as this could result in serious damage to the sensor.•Never immerse the RVG sensor control box in any solution.•Disinfect the sensor head after each patient.•Do not use chemical autoclave for the toothbrush holders and avoid direct contact with the metallic part of the autoclave.•To prevent cross-contamination, use a new hygienic barrier for each new patient.
6 Chapter 1  Safety InformationMarking and Labeling SymbolsType BF device symbol complying with the IEC 60601-1 standardIn the EEC, this symbol indicates: DO NOT discard this product in a trash receptacle; use an appropriate recovery and recycling facility.Contact your local sales representative for additional information on the collection and recovery programs available for this productWarning: General warning signThe ON/OFF button General mandatory action signFollow operating instructions signNon-ionizing radiationManufactured DateManufacturer’s address
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed02 7Label LocationsThe following Figures illustrate the label locations of the KODAK RVG 6500 Systems.Figure 1 KODAK RVG 6500 Control Box LabelFigure 2 KODAK RVG 6500 LabelsFigure 3 KODAK RVG 6500 IPS Aiming Ring LabelModel Number: Kodak RVG6500FCC ID   : U72RVG00002IC  : 7027A-RVG00002**IPS
8 Chapter 1  Safety InformationKODAK RVG 6500 With or Without IPS System Battery SpecificationThe KODAK RVG 6500 with or without IPS System provides a medical battery charge. You can purchase additional battery separately (for battery replacement, see Chapter “Maintenance” section “Replacing the RVG Battery”). •A battery is required for wireless use.•Minimum battery life is 500 charge and discharge cycles where the cell capacity remains above 80% of initial capacity.•New battery provides approximately 90 image acquisitions (3.0 hrs heavy usage).•A battery charge state is indicated on the Acquisition Interface. The detector determines if the installed battery is not properly charging, and provides this battery status to the Acquisition Interface.Important:  To ass ure  pro pe r operation, use only the KODAK RVG 6500 with or without IPS System battery.
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed02 92 Regulatory InformationGeneral Regulatory InformationCompliance with European and International StandardsEN 60601-1 / IEC 60601-1Medical Electrical Equipment, Part 1 : General requirements for basic safety and essential performanceEN 60601-1-2 / IEC 60601-1-2Medical Electrical Equipment, Part 1-2 :General requirements for basic safety and essential performance - Collateral Standard : Electromagnetic CompatibilityEN 60601-1-3 / IEC 60601-1-3Medical Electrical Equipment, Part 1-3 : General requirements for basic safety and essential performance - Collateral Standard : Radiation protection in diagnostic X-ray equipmentEN 60601-1-6 / IEC 60601-1-6Medical Electrical Equipment, Part 1-6 : General requirements for basic safety and essential performance - Collateral Standard :UsabilityEN ISO 14971 Medical devices - Application of risk management to medical devices EN 980 Symbols for use in the labeling of medical devicesEN 1041 Information supplied by the manufacturer of medical devicesEN 62304/IEC 62304 Medical device software - Software life cycle processesEN 10993-1 Biological evaluation of medical devices - Part 1 : Evaluation and testingEN 300 328 Electromagnetic Compatibility and Radio Spectrum Matters
10 Chapter 2  Regulatory InformationEN 302 291-2Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Close Range Inductive Data Communication equipment operating at 13,56 MHz; Part 2: Harmonized EN under article 3.2 of the R&TTE DirectiveEN 301 489-1Electromagnetic compatibility and Radio spectrum Matters (ERM); ElectroMagnetic Compatibility (EMC) standard for radio equipment and services; Part 1: Common technical requirementEN 301 489-3Electromagnetic compatibility and Radio spectrum Matters (ERM); ElectroMagnetic Compatibility (EMC) standard for radio equipment and services; Part 3: Specific conditions for Short-Range Devices (SRD) operating on frequencies between 9kHz to 40GHzEN 301 489-17ElectroMagnetic Compatibility and Radio Spectrum Matters (ERM); ElectroMagnetic Compatibility (EMC) Standard for Radio Equipment and Services; Part 17 : Specific Conditions for 2,4 GHz Wide band Transmission Systems and 5 GHz High Performance RLAN EquipmentEN 50364Limitation of human exposure to electromagnetic fields from devices operating in the frequency range 0Hz to 300GHz, used in electronic article surveillance (EAS), radio frequency identification (RFID) and similar applicationsEN 50371Generic Standard to demonstrate the compliance of low power electronic and electrical apparatus with the basic restrictions related to human exposure to electromagnetic fields (10 MHz - 300 MHz). General PublicClassification in Accordance with EN/IEC 60601-1Type of protection against electric shock Class 1 equipmentDegree of protection against electric shock Typ e B FCompliance with European and International Standards
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed0211•Medical electrical equipment requires special precautions regarding electromagnetic compatibility (EMC).•KODAK RVG 6500 with or without IPS System must be installed and put into service according to the EMC information provided in this document.•Communication Equipment: Portable and mobile Radio Frequency (RF) communications equipment can affect the Electromagnetic Compatibility of KODAK RVG 6500 with or without IPS System.•KODAK RVG 6500 with or without IPS System may be interfered with other equipment even if that other equipment complies with CISPR emission requirements.Protection against harmful ingress of water Ordinary equipmentOperation mode Continuous operation Flammable anesthetics Not suitable for use in presence of flammable anesthetics or a mixture of flammable anesthetics with air or oxygen or nitrous oxideConformity with EN/IEC 60601-1-3 Attenuation equivalent for the enclosure of the image receiver unit (at 100 kV)0.2 mm eq. AIKODAK RVG 6500 With or Without IPS System ComponentsRVG sensor and the control boxMedical power supply Model: MW172KB0500F02Mains outlet cable: 2.50 meterWiFi access point WGR614IPS aiming ringClassification in Accordance with EN/IEC 60601-1
12 Chapter 2  Regulatory Information•Use limitation: the use of accessories, cables, or transducers other than those specified in this document with the exception of cables, accessories or transducers sold by Carestrem health as replacement parts of internal components, may result in increased emissions or decreased immunity of the KODAK RVG 6500 with or without IPS System.•The KODAK RVG 6500 with or without IPS System should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the KODAK RVG 6500 with or without IPS System should be observed to verify normal operation in the configuration in which it will be used.Guidance and Manufacturer’s Declaration - Electromagnetic Emissions (IEC 60601-1-2) The KODAK RVG 6500 with or without IPS System is intended for use in the electromagnetic environment specified below. The customer or the user of the KODAK RVG 6500 with or without IPS System should assure that it is used in such an environment. Emissions Test Compli-ance Electromagnetic Environment - GuidanceRF emissions CISPR 11 Group 1The KODAK RVG 6500 with or without IPS System uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.RF emissions CISPR 11 Class BThe KODAK RVG 6500 with or without IPS System is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.Harmonic emissionsIEC 61000-3-2Class AVoltage fluctuations/flicker emissionsIEC 61000-3-3Complies
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed0213Guidance and Manufacturer’s Declaration - Electromagnetic Immunity The KODAK RVG 6500 with or without IPS System is intended for use in the electromagnetic environment specified below. The customer or the user of the KODAK RVG 6500 with or without IPS System should assure that it is used in such an environment. Immunity Test IEC 60601 Test Level Compliance Electromagnetic Environment - GuidanceElectrostatic discharge (ESD)IEC 61000-4-2 ±6 kV contact±8 kV air ±6 kV contact±8 kV airFloors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.Electrical fast transient/burstIEC 61000-4-4 ±2 kV for power supply lines±1 kV for input/output lines ±2 kV for power supply lines±1 kV for input/output linesMains power quality should be that of a typical commercial or hospital environment.SurgeIEC 61000-4-5 ±1 kV line(s) to line(s)±2 kV line(s) to earth ±1 kV line(s) to line(s)Not applicableMains power quality should be that of a typical commercial or hospital environment.Voltage dips, short interruptions and voltage variations on power supply input linesIEC 61000-4-11<5% UT (>95% dip in UT)for 0,5 cycle40% UT (60% dip in UT)for 5 cycles70% UT (30% dip in UT)for 25 cycles<5% UT (>95% dip in UT)for 5 sec<5% UT (>95% dip in UT)for 0,5 cycle40% UT (60% dip in UT)for 5 cycles70% UT (30% dip in UT)for 25 cycles<5% UT (>95% dip in UT)for 5 secMains power quality should be that of a typical commercial or hospital environment. If the user of the KODAK RVG 6500 with or without IPS System requires continued operation during power mains interruptions, it is recommended that the KODAK RVG 6500 with or without IPS System be powered from an uninterruptible power supply or a battery.Power frequency (50/60 Hz) magnetic fieldIEC 61000-4-83 A/m 3 A/mPower frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environmentNOTE: UT is the a.c. mains voltage prior to application of the test level.
14 Chapter 2  Regulatory InformationGuidance and Manufacturer’s Declaration - Electromagnetic Immunity (IEC 60601-1-2) The KODAK RVG 6500 with or without IPS System is intended for use in the electromagnetic environment specified below. The customer or the user of the KODAK RVG 6500 with or without IPS System should assure that it is used in such an environment. Immunity TestIEC 60601 Test LevelCompliance LevelElectromagnetic Environment - GuidanceConducted RF IEC 61000-4-6Radiated RFIEC 61000-4-33 Vrms150 kHz to 80 MHz 3 V/m80 MHz to 2,5 GHz[V1]= 3 V[E1]= 3 V/mPortable and mobile RF communications equipment should be used no closer to any part of the KODAK RVG 6500 with or without IPS System, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distancewhere P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m).Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey should be less than the compliance level in each frequency range.b Interference may occur in the vicinity of equipment marked with the following symbol:NOTE 1:  At 80 MHz and 800 MHz, the higher frequency range applies.NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the KODAK RVG 6500 with or without IPS System is used exceeds the applicable RF compliance level above, the KODAK RVG 6500 with or without IPS System should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the KODAK RVG 6500 with or without IPS System.b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed0215Recommended Separation Distances between Portable and Mobile RF Communications Equipment and the KODAK RVG 6500 System (IEC 60601-1-2)The KODAK RVG 6500 with or without IPS System is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the KODAK RVG 6500 with or without IPS System can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the KODAK RVG 6500 with or without IPS System as recommended below, according to the maximum output power of the communications equipment.Rated Maximum Output Power of Transmitter WSeparation Distance According to Frequency of Transmitter150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz0.01 0.12 0.12 0.230.1 0.38 0.38 0.731 1.2 1.2 2.310 3.8 3.8 7.3100 12 12 23For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.Note:  The communication without breaking has been determined to be essential performance with regard to electromagnetic compatibility
16 Chapter 2  Regulatory InformationCompliance with International Regulations•The KODAK RVG 6500 with or without IPS System is an active device specifically intended for recording of X-ray diagnostic image. Medical Device directives 93/42/ European Economic Community (EEC), Class IIa follow the rule 16.•Radio and Telecommunications Terminal Equipment directives 1999/5/EEC•FCC rules part 15•Medical Devices Regulations (Canada)FCC Requirements for USAKODAK RVG 6500 System and KODAK RVG 6500 IPS System WARNING TO USERS IN THE UNITED STATESFederal Communication Commission Interference Statement 47 CFR Section 15.105(b) This equipment has been tested and found compliant with the limits for a Class B digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that the interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures: •Reorient or relocate the receiving antenna. •Increase the separation between the equipment and receiver. •Connect the equipment into an outlet on a circuit different from that to which the receiver is connected. •Consult the dealer or an experienced radio/TV technician for help. No Unauthorized Modifications47 CFR Section 15.21CAUTION: This equipment may not be modified, altered, or changed in any way without signed written permission from Carestream. Unauthorized modification may void the equipment authorization from the FCC and will void the Carestream warranty.Antenna Requirement47 CFR Section 15.203This device KODAK RVG 6500 System and KODAK RVG 6500 IPS System complies with Part 15 of the FCC Rules. Operation is subject to the following 2 conditions: (1) This device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed0217IC Requirements for Canada Operation is subject to the following 2 conditions: (1) This device may not cause interference, and (2) this device must accept any interference, including interference that may cause undesired operation of the device.To reduce potential radio interference to other users, the antenna type and its gain should be so chosen that the equivalent isotropically radiated power (e.i.r.p.) is not more than that permitted for successful communication.L'utilisation de ce dispositif est autorisée seulement aux deux conditions suivantes : (1) il ne doit pas produire de brouillage, et (2) l'utilisateur du dispositif doit être prêt à accepter tout brouillage radioélectrique reçu, même si ce brouillage est susceptible de compromettre le fonctionnement du dispositif.Afin de réduire le risque d'interférence aux autres utilisateurs, il faut choisir le type d'antenne et son gain de façon à ce que la puissance isotrope rayonnée équivalente (p.i.r.e.) ne soit pas supérieure au niveau requis pour l'obtention d'une communication satisfaisante. Cet appareil numérique de la classe B respecte toutes les exigences du règlement sur le matériel brouilleur du Canada.
18 Chapter 2  Regulatory InformationDeclaration of Conformity with the R-TTE Directives
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed023 Technic al SpecificationsFactoryTROPHY4, Rue F. Pelloutier, Croissy-Beaubourg77435 Marne la Vallée Cedex 2, FranceManufacturer: Carestream health, Inc.150 Verona StreetRochester,New York - USA 14608ModelKODAK RVG 6500 SystemKODAK RVG 6500 IPS SystemKODAK RVG 6500 With or Without IPS System Technical SpecificationsComponents KODAK RVG 6500 SystemKODAK RVG 6500 IPS SystemRVG SensorSensor Technol ogy CMOS CMOSSensor matrix⟨Size 0: 900 x 1200 pixels⟨Size 1:1200 x 1600 pixels⟨Size 2: 1440 x 1920 pixels⟨Size 1:1200 x 1600 pixels⟨Size 2: 1440 x 1920 pixels
20 Chapter 3  Technical SpecificationsSensor active surface dimensions⟨Size 0: 16.6 x 22.2 mm⟨Size 1: 22.2 x 29.6 mm⟨Size 2: 26.6 x 35.5 mm⟨Size 1: 22.2 x 29.6 mm⟨Size 2: 26.6 x 35.5 mmGray scale 4096 bits 4096 bitsRVG Control BoxDimension 83mm (H) x 47mm (W) x 16mm (D)83mm (H) x 47mm (W) x 21mm (D)Weight 65g 90gBattery type Lithium LithiumBattery charging time 4hrs 4hrsRVG Control Box ChargerMains power supply Input voltage⟨230/240 V - 50/60 Hz⟨100/110/130 V - 50/60 Hz⟨230/240 V - 50/60 Hz⟨100/110/130 V - 50/60 HzWiFi Access PointReference Model WGR614 WGR614Dimension 28 x 175 x 119 mm 28 x 175 x 119 mmWeight 260 g 260 gInput voltage 100/240 V - 50/60 Hz 100/240 V - 50/60 HzIPS aiming ringTechnology NA Electromagnetic signalsDimensions NA 150 x 115 x 40 mmWeight NA 235 gBattery type NA 4 x AAAA (Continued)Components KODAK RVG 6500 SystemKODAK RVG 6500 IPS System
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed0221Minimum Computer System RequirementThe computer and the peripheral equipment must conform to theIEC60950 standard. Item Viewing and Acquisition  CommentsCPU 2 GHz Intel Duo CoreRAM 2 GBRAM has a major impact on system performance.Hard disk drive•1.2 GB for software installation •80 GB free space to use the softwareGraphic board Graphic board supporting Open GL 1.2 with 256 MB of video RAM (Recommended Nvidia / ATI)The video RAM has major impact on system performance.Monitor•1 monitor•17” or larger•1024 x 768 minimum screen resolution - 32 bits color modeYour monitor is a vital component in displaying quality images. Low-quality screens will prevent you from proper diagnoses and treatment.Operating system •Windows XP Home / Pro edition SP3 (32 bits)•Windows Vista (32 bits) (Recommended SP1)•Windows 7 (32 or 64 bits)The operating system specifications are valid as of KODAK Dental Imaging Software v6.12.Ethernet interface 100 Mbits for LAN USB 2.0 2 portsWireless adapter Wireless 802.11g Adapter (USB, PCMCIA or PCI)CD/DVD drive DVD-ROM drive is required to install the product.Backup media Removable/portable, external hard disk drive.We strongly recommend a daily backup of x-ray images and patient records.
22 Chapter 3  Technical SpecificationsRFID Technical SpecificationWiFi Network Technical SpecificationItem  SpecificationFrequency band 13.56MHzStandard classification ISO 14443Transmission range <2cmItem  SpecificationNetwork Protocol TCP/IPNetwork Type Private Wireless LAN (WLAN)Network Mode Infrastructure modeWireless Protocol  802.11gFrequency band 2.4 GHz ISM radio bandModulation OFDMData rated (measured) Up to 10MbpsNumber of channels•11 for USA & Canada•13 for Europe•14 for JapanMaximum Power 20 mWIP AddressThe KODAK RVG 6500 / KODAK RVG 6500 IPS client acts as a DHCP. Client DHCP server is embedded within the Access Point.Data Size (maximum) One 5.4 MByte fileSecurityWEP 128-bit encryption Factory loaded keyPrivate Patient Identification Data No patient ID data transmitted
KODAK RVG 6500 System_Regulatory User Guide (SM737)_Ed0223KODAK RVG 6500 With or Without IPS System Environmental RequirementsEnvironmental SpecificationsOperating temperature 0° to 40° CRange Up to 10mAmbient Operating ConditionsTem pe ra tures 0 ~ 40°CRelative humidity 45% ~ 85%Atmospheric pressure 700 ~ 1060 hpaStorage ConditionsTem pe ra tures -20 ~ 60 °CRelative humidity 45 ~ 85%Atmospheric pressure 700 ~ 1060 hpaTransport ConditionsTem pe ra tures -20 ~ 60 °CRelative humidity 45 ~ 85%Atmospheric pressure 700 ~ 1060 hpa
24 Chapter 3  Technical Specifications

Navigation menu