U726850Image Transmitter

DRYVIEW 6850 Laser Imager User’s Guide 150 Verona Street Rochester, New York 14608 © Carestream Health, Inc., 2010 CARESTREAM and DRYVIEW are trademarks of Carestream Health, Inc. The Kodak trademark and trade dress are used under license from Kodak. Pub No. 2G8647 Rev. A i Table of Contents 1 Overview 6850 Laser Imager ........................................................................................................................................... 1-1 Intended Use .................................................................................................................................................... 1-1 System Components ......................................................................................................................................... 1-2 How the Laser Imager Works ........................................................................................................................... 1-3 Film Throughput .............................................................................................................................................. 1-4 Agency Compliance .......................................................................................................................................... 1-4 User Guide Conventions ................................................................................................................................... 1-4 2 Using and Maintaining the Imager Operator Control of the Imager ........................................................................................................................ 2-1 Turning Imager Power ON and OFF.................................................................................................................. 2-1 Power ON................................................................................................................................................... 2-2 Normal Power OFF ............................................................................................................... ...................... 2-2 Emergency Power OFF ............................................................................................................................... 2-2 Power Failures ........................................................................................................................................... 2-3 Power Save................................................................................................................................................. 2-3 Using the Touch Screen.................................................................................................................................... 2-3 Touch Screen Functions ............................................................................................................................. 2-4 Touch Screen Help..................................................................................................................................... 2-5 General Help ........................................................................................................................................ 2-6 Specific Screen Help ............................................................................................................................ 2-6 Installation Road Map ...................................................................................................................................... 2-6 Physical Setup ............................................................................................................................................ 2-6 Configuration .................................................................................................................. ........................... 2-6 Imager Passcode .............................................................................................................................................. 2-7 Loading and Removing the Film Cartridges....................................................................................................... 2-8 Drawers and Doors .......................................................................................................................................... 2-9 Opening Film Drawers and Main Door ....................................................................................................... 2-9 Opening the Film Registration Door ........................................................................................................... 2-9 Opening Air Intake Door ............................................................................................................................ 2-9 Film Drawers and Main Door Manual Override Latch...............................................................................2-10 Filter Maintenance ......................................................................................................................................... 2-11 Cleaning the Electronics Filter .................................................................................................................. 2-11 ii Changing the PMM ................................................................................................................................... 2-11 3 Troubleshooting Overview .......................................................................................................................................................... 3-1 Error and Alarm Indications ............................................................................................................................ 3-1 Correcting Errors....................................................................................................................................... 3-1 Correcting Film Jams With the Imager Powered ON ................................................................................... 3-2 Correcting Film Jams With the Image…

Text truncated - open the document above for the full version.

DRYVIEW 6850 Laser Imager Safety Manual 150 Verona Street Rochester, New York 14608 © Carestream Health, Inc., 2010 CARESTREAM and DRYVIEW are trademarks of Carestream Health, Inc. Pub No. 2G8646 Rev. A i Table of Contents Safety and Related Information Safety, Warnings, and Cautions .....................................................................................................1 Safety Labels .............................................................................................................................5 Safety and Health Compliance.....................................................................................................11 Safety.......................................................................................................................................11 EMC ........................................................................................................................................12 EU Directives ..........................................................................................................................17 CE Marking .............................................................................................................................17 Please Note ..............................................................................................................................18 Imager Specifications ...................................................................................................................18 Publication History .......................................................................................................................18 2010-11-042G86461 Safety and Related Information Safety, Warnings, and Cautions Please read and understand all instructions before using this product. RISK OF ELECTRIC SHOCK: This equipment is operated with hazardous voltage which can shock, burn, or cause death. • Remove wall plug before servicing equipment. Never pull on cord to remove from outlet. Grasp plug and pull to disconnect. Do not attempt to service or repair the laser imager yourself to avoid exposure to dangerous voltage, laser beam, or other danger. Always call an Authorized Service Provider of Carestream Health, Inc. products for any service or repair. • Do not operate equipment with a damaged power cord. • Do not use an extension cord to power this equipment. • Do not operate equipment with any of the safety interlocks overridden. • Position the power cord so it will not be tripped over or pulled. • Connect this equipment to a grounded wall outlet. • Four power cord sets are provided with this equipment: – power cord with plug for use in North America – power cord with plug for use in China – power cord with plug for use in the United Kingdom – power cord with plug for use in Europe All other countries must use an Agency-approved power cord with plug type suitable for the country of use, or contact an authorized Carestream Health, Inc. dealer. DANGER: THIS EQUIPMENT CONTAINS MOVING PARTS THAT MAY BE ACCESSIBLE TO THE USER. LOOSE CLOTHING, JEWELRY OR LONG HAIR MAY CAUSE PERSONAL INJURY OR DAMAGE TO THE EQUIPMENT. • Do not operate equipment with the covers open. 22G86462010-11-04 Safety and Related Information DANGER: THIS EQUIPMENT IS NOT CONTAINED IN A SEALED CABINET. DO NOT USE THIS EQUIPMENT IN LOCATIONS WHERE IT CAN COME IN CONTACT WITH LIQUIDS, INCLUDING BODY FLUIDS. CAUTION: Do not use a cell phone within 2 meters of a laser imager. This proximity includes any imager behind a wall adjacent to your location. CAUTION: Do not use a microwave oven within 4 meters of a laser imager. Electromagnetic radiation from a microwave oven is only an issue if after the oven door is closed and latched, the seal does not maintain an electromagnetic tight fit between the oven door and oven main housing. Determining if the seal has an electromagnetic tight fit requires special detection equipment. CAUTION: Do not use in the presence of flammable anesthetics, oxygen, or nitrous oxide. This equipment does not have a gas-sealed electronics enclosure and could ignite any flammable or explosive gases present in its environment. CAUTION: This equipment uses a DICOM network port, and is intended to connect to other medical devices. It is not intended to be connected directly outside the building. Only an Authorized Service Provider of Carestream Health, Inc., products or customer’s qualified service personnel may perform installation and service maintenance. CAUTION: This device should not be used in close contact with MRI devices, due to possible very high magnetic fields near an MRI unit. The magnetic field in the area where this equipment is installed must be less than 50 Gauss. CAUTION: Do not substitute or modify any part of this equipment without prior written approval of Carestream Health, Inc. CAUTION: Federal law prohibits dispensing without a prescription. Safety and Related Information 2010-11-042G86463 CAUTION: 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. These limits are designed to provide reasonable protection against harmful interference when the equipment is operated in a commercial environment. This equipment generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with the User Guide and other User Documentation, may cause harmful interference to radio communications. Operation of this equipment in a residential area is likely to cause harmful interference in which case the user will be required to correct the interference at his own expense. CAUTION: Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment. CAUTION: Do not use isopropyl alcohol to clean the exterior surfaces of the laser imager. Isopropyl alcohol can dissolve the exterior paint on the laser imager. CAUTION: In the U.S., e…

Text truncated - open the document above for the full version.

TÜV SÜD America Inc. Phone: (651) 638-0297 19333 Wild Mountain Road Fax: (651) 638-0298 Taylor Falls, MN 55084 E-mail: [email protected] www.TUVamerica.com Management Service • Product Service • Industry Service • Automotive • BABT TÜV America Inc. is a subsidiary of TÜV SÜD Group. TÜV SÜD AMERICA INC 19333 WILD MOUNTAIN ROAD TAYLORS FALLS, MINNESOTA 55084-1786 ENGINEERING STATEMENT For Certification of Carestream Health Incorporated Laser Imaging System Model No: DRYVIEW 6850 Laser Imaging System FCC ID: U726850 FRN: 0016195265 IC: 7027A-6850 I am an Electromagnetic Compatibility Engineer for TÜV SÜD AMERICA INC, Taylors Falls, Minnesota. My education and experience are a matter of record with the Federal Communications Commission. TÜV SÜD AMERICA INC has been authorized by Ronald C Cain, EMC Compliance Engineer, of Carestream Health Incorporated, to make Certification measurements of the above mentioned equipment. I attest that all testing done under my supervision was done in accordance with, and that the EUT fulfills the requirements of, the Federal Communications Commission's CFR 47 Part 15.209 and Industry Canada's RSS-210 Issue 7. Joel T. Schneider Senior Engineer Minnesota Wild River Lab TÜV SÜD America Product Service Tel: 651 604 4582 Fax: 651 638 0298 [email protected] Dated: 30 November 2010

earn Authorityto Act as Agent Date:10/25/2010 AmericanTelecommunicationCertificationBody,Inc. 6731 WhittierAvenue Suite ClIO McLean,VA 22101 To WhomIt May Concern: TUV SUD Americais authorizedto act on our behalf,until otherwisenotified,for applicationsto AmericanTelecommunicationCertificationBody,Inc. (ATCB). We certifythat we are not subjectto denialof federalbenefits,that includesFCC benefits,pursuantto Section5301 of the Anti-DrugAbuseAct of 1988,21U.S.C.862. Further,no party, as definedin 47 CFR 1.2002(b), to the applicationis subjectto denialof federalbenefits,that includesFCC benefits. Thankyou, AgencyAgreementExpirationDate: 10/1/2011 By: RonaldL. Cain (Print name) Title:EMC ComplianceEngineer On behalfof: CarestreamHealthInc. (CompanyName) Telephone: 585-627-8321 1 _ Must be signedby applicantcontactgiven for applicanton the FCC site, or by the authorizedagent if an appropriate authorizedagent letter has been provided.Lettersshouldbe placedon appropriateletterhead. 081710-4

Requestfor Confidentiality Date:10/2512010 Subject:ConfidentialityRequestfor: CarestreamHealthInc. U72-6850& 7027A~6850 Pursuantto FCC 47 CRF 0.457(d)and 0.459 and IC RSP-100,Section10, the applicantrequeststhat a part of the subjectFCC applicationbe held confidential. oPermanent*2 X Permanent DPermanent DPermanent X Permanent Type of ConfidentialityRequested D Short TermX Permanent DShort Term D Short Term DShort Term DShort Term DShort Term D Short Term D Short Term DShort TermDPermanent* *Note:(InsertExplanationas Necessary) Exhibit Block Diagrams ExternalPhotos InternalPhotos OperationDescription/Theoryof Operation Parts List & Placement/BOM Tune-UpProcedure Schematics Test Setup Photos User'sManual CarestreamHealthInc. has spent substantialeffort in developingthis productand it is one of the first of its kind in industry.Havingthe subjectinformationeasily availableto "competition"wouldnegatethe advantagethey have achievedby developingthis product.Not protectingthe detailsof the designwill result in financialhardship. PermanentConfidentiality: The applicantrequeststhe exhibitslisted above as permanentlyconfidentialbe permanentlywithheldfrom public reviewdue to materialsthat containtrade secretsand proprietaryinformationnot customarilyreleasedto the public. Short-TermConfidentiality: The applicantrequeststhe exhibitsselectedabove as short term confidentialbe withheldfrom publicview for a periodof (specifynumberof days not to exceed180)3_days from the date of the Grant of Equipment Authorizationand prior to marketing.This is to avoid prematurereleaseof sensitiveinformationprior to marketing or releaseof the productto the public.Applicantis also aware that they are responsibleto notify ATCB in the event informationregardingthe productor the productis made availableto the public.ATCBwill then releasethe documentslisted above for publicdisclosurepursuantto FCC PublicNoticeDA 04-1705. NOTEfor IndustryCanadaApplications: The applicantunderstandsthat until such time that IC distinguishesbetweenShort Term and Permanent Confidentiality,either type of markedexhibitabove will simplybe markedConfidentialwhen submittedto IC. Sincerely, By: ~L~'J/EMC ComplianceEngineer (Signature/Title4) RonaldL. Cain (Print name) 2 _ The asteriskeditems (*) requirefurtherjustificationbefore permanentconfidentialitywill be allowed.These also currently requirereviewby the FCC under their Permit-But-Askpolicy before the grant is issued and can delay completionof an application.Furtherjustificationshouldbe added to the note above.One such examplefor a potted device would be: "The EUT is FULLYpotted using a non-removableepoxy based material.Removalof pottingmaterialcauses irreparable damageto internalcircuitry.Seephotographsexhibitsthat outlinethe device before and after potting." 3 ~Please refer to http://atcb.com/publicdocs/Memo-Short-Term-Vs-Standard-Confidentiality.pdffor completedetails. 4 _ Must be signed by applicantcontactgiven for applicanton the FCC site, or by the authorizedagent if an appropriate authorizedagent letter hasbeen provided.Lettersshouldbe placedon appropriateletterhead. 081710- 4

DryView 6850 External Photos TOP VIEW BOTTOM VIEW – It can have 6 or 4 wheels both are UL approved. REAR VIEW LEFT SIDE RIGHT SIDE FRONT

DryView 6850 Laser Imaging System – Internal Photos Film Drawer with RF-Tag Antenna Top (Dark Green / Black) Rectangle Film Drawer with RF-Tag Bottom RF-Tag Antenna Board Top RF-Tag Antenna Board Bottom Transmitter Board Top Transmitter Board Bottom

TÜV SÜD AMERICA INC 19333 Wild Mountain Road Taylors Falls MN 55084 Tel: (651) 638-0297 Fax: (651) 638-0298 Rev. 113006 TEST RESULT SUMMARY FCC Part 15 Subpart C Section 15.207 FCC Part 15 Subpart C Section 15.209 IC RSS-210 Issue 7 IC RSS-Gen Issue 2 MANUFACTURER'S NAME Carestream Health Incorporated 150 Verona Street Rochester NY 14608 PRODUCT NAME DRYVIEW 6850 Laser Imaging System MODEL NUMBER(S) TESTED DRYVIEW 6850 Laser Imaging System SERIAL NUMBER(S) TESTED EM 06 PRODUCT DESCRIPTION Laser Imager with a product class 1, 13.56 MHz RFID TEST REPORT NUMBER WC1000098.2 Rev A TEST DATE(S) 28 January 2010 TÜV SÜD America Inc, as an independent testing laboratory, declares that the equipment tested as specified above conforms to the applicable EMC requirements of FCC Part 15 Subpart C Sections 15.207 “Conducted Limits” and 15.209 “Radiated emission limits; general requirements” and IC RSS-210 Issue 7 “Low-power Licence-exempt Radiocommunication Devices (All Frequency Bands): Category I Equipment” and IC RSS-Gen “General Requirements and Information for the Certification of Radiocommunication Equipment”. It is the manufacturer's responsibility to assure that additional production units of this model are manufactured with identical electrical and mechanical characteristics. Any modifications necessary for compliance made during testing on the above mentioned date(s) must be implemented in all production units for compliance to be maintained. Date: 18 June 2010 Location: Taylors Falls MN Robert J Behringer Joel T Schneider USA EMC Test Engineer Senior EMC Engineer Not Transferable TÜV SÜD AMERICA INC 19333 Wild Mountain Road Taylors Falls MN 55084 Tel: (651) 638-0297 Fax: (651) 638-0298 Rev. 113006 EMC TEST REPORT Test Report No. WC1000098.2 Rev A Date of issue: 18 June 2010 Product Name DRYVIEW 6850 Laser Imaging System Model(s) Tested DRYVIEW 6850 Laser Imaging System Serial No(s) Tested EM 06 Product Description Laser Imager with 13.56 MHz RFID Manufacturer Carestream Health Incorporated 150 Verona Street Rochester NY 14608 Test Result „ Positive † Negative TÜV SÜD America Inc reports apply only to the specific samples tested under stated test conditions. It is the manufacturer's responsibility to assure that additional production units of this model are manufactured with identical electrical and mechanical components. TÜV SÜD America Inc shall have no liability for any deductions, inferences or generalizations drawn by the client or others from TÜV SÜD America Inc issued reports. This report is the confidential property of the client. As a mutual protection to our clients, the public and ourselves, extracts from the test report shall not be reproduced except in full without our written approval. This report shall not be used by the client to claim product endorsement by NVLAP, NIST, or any agency of the US government. TÜV SÜD America Inc and its professional staff hold government and professional organization certifications and are members of AAMI, ACIL, AEA, ANSI, IEEE, NARTE, and VCCI. Test Report WC1000098.2 Rev A1 of 34 TÜV SÜD AMERICA INC 19333 Wild Mountain Road Taylors Falls MN 55084 Tel: (651) 638-0297 Fax: (651) 638-0298 Rev. 113006 REVISION RECORD REVISION TOTAL NUMBER OF PAGES DATE DESCRIPTION 34 17 February 2010 Initial Release A 34 18 June 2010 Revisions Include: ƒ Page 1 and corresponding TRS: Correcting the Test Report Number from WC1000089.2 to WC1000098.2. Changing model number from CARESTREAM DRYVIEW 6850 Laser Imager to DRYVIEW 6850 Laser Imaging System and Name of Equipment from DRYVIEW 6850 Laser Imager to DRYVIEW 6850 Laser Imaging System per information received from Carestream. ƒ Appendix B: Replaced with revised document received from Carestream. Test Report WC1000098.2 Rev A2 of 34 TÜV SÜD AMERICA INC 19333 Wild Mountain Road Taylors Falls MN 55084 Tel: (651) 638-0297 Fax: (651) 638-0298 Rev. 113006 D I R E C T O R Y Contents Revision Record 2 Directory 3 Test Regulations 4 Environmental Conditions 4 Power Supply 4 Test Equipment Traceability 4 Test Information General Field Strength Limits 0.009 – 30 MHz FCC 15.209(a) & (c), IC RSS-210 2.6 5 Radiated Emissions 30 - 5000 MHz 15.209(c) & (f) , IC RSS-210 2.6 6 - 8 Occupied Bandwidth RSS-Gen 4.6.1 9 - 11 Conducted limits - AC Power Lines 15.207(a), IC RSS-Gen 7.2.2 12 - 13 Test area diagram 14 Test-setup Photos 15 - 18 Equipment Under Test Information 19 General Remarks, Deviations, Summary 20 Appendix A Carestream Health Incorporated EMC Test Plan, Document Part Number #8F6226 21 - 32 Appendix B Measurement Protocol 33 - 34 Test Report WC1000098.2 Rev A3 of 34 TÜV SÜD AMERICA INC 19333 Wild Mountain Road Taylors Falls MN 55084 Tel: (651) 638-0297 Fax: (651) 638-0298 Rev. 113006 EMC TEST REGULATIONS: The tests were performed according to the following regulations: FCC Part 15 Subpart C Section 15.207 Paragraph (a) FCC Part 15 Subpart C Section 15.209 Paragraphs (a), (c), (f) IC RSS-210 Issue 7 Section 2.6 IC RSS-Gen Issue 2 Sections 4.6.1, 7.2.2 ENVIRONMENTAL CONDITIONS IN THE LAB Actual Temperature: : 22°C Atmospheric pressure : 100kPa Relative Humidity : 16% POWER SUPPLY UTILIZED Power supply system : 110 V / 60 Hz TEST EQUIPMENT All measurement instrumentation is traceable to the National Institute of Standards and Technology and is calibrated according to internal procedure. SIGN EXPLANATIONS † - not applicable „ - applicable Test Report WC1000098.2 Rev A4 of 34 TÜV SÜD AMERICA INC 19333 Wild Mountain Road Taylors Falls MN 55084 Tel: (651) 638-0297 Fax: (651) 638-0298 Rev. 113006 General field strength limits 0.009 – 30 MHz FCC 15.209(a), FCC 15.209(c), IC RSS-210 2.6 Test summary The requirements are: „ - MET † - NOT MET Testing was performed in accordance with the test procedure of ANSI C63.4 2003, clause 8.2.2 Maximum field strength of the fundamental is -7.5 dBμV/m* or 0.42 μV/m at 30 meters at 13.56 MHz Minimum margin of compliance of the fundamental is 37 dB Maximum field strength of spurious emissions is…

Text truncated - open the document above for the full version.

TÜV SÜD AMERICA INC 19333 Wild Mountain Road Taylors Falls MN 55084 Tel: (651) 638-0297 Fax: (651) 638-0298 Rev. 113006 TEST SETUP FOR EMISSIONS TESTING WILD RIVER LAB Large Test Site Notes: 1. Items shown in dotted lines are located on the floor below the test area. It is 5 meters vertically from the ground floor to the test area. 2. 50 Hz, 60 Hz, and 400 Hz are power panels for alternating current. 3. The antenna may be positioned horizontally 3, 10 or 30 meters from the center of the turntable. 4. The circle is a 6.7 meter diameter turntable. 5. A ground plane is in the plane of this sheet. 6. The test sample is shown in the azimuthal position representing zero degrees. EUT 0 90270 180 60 Hz 50 Hz 400 Hz Shielded Enclosure ANTENNA Test Report WC1000098.2 Rev A14 of 34 TÜV SÜD AMERICA INC 19333 Wild Mountain Road Taylors Falls MN 55084 Tel: (651) 638-0297 Fax: (651) 638-0298 Rev. 113006 Test-setup photo(s): General Field Strength Limits 0.009 – 30 MHz Test Report WC1000098.2 Rev A15 of 34 TÜV SÜD AMERICA INC 19333 Wild Mountain Road Taylors Falls MN 55084 Tel: (651) 638-0297 Fax: (651) 638-0298 Rev. 113006 Test-setup photo(s): Radiated Emissions 30 - 8000 MHz Test Report WC1000098.2 Rev A16 of 34 TÜV SÜD AMERICA INC 19333 Wild Mountain Road Taylors Falls MN 55084 Tel: (651) 638-0297 Fax: (651) 638-0298 Rev. 113006 Test-setup photo(s): Radiated Emissions 30 - 8000 MHz Test Report WC1000098.2 Rev A17 of 34 TÜV SÜD AMERICA INC 19333 Wild Mountain Road Taylors Falls MN 55084 Tel: (651) 638-0297 Fax: (651) 638-0298 Rev. 113006 Test-setup photo(s): Conducted Emissions, AC lines, 150 kHz - 30 MHz Test Report WC1000098.2 Rev A18 of 34