2AAPD-SPECTRASTMultistainer

HistoCore SPECTRA ST Stainer The Pathology Company Instructions for Use English Order No. 14 0512 80101 - Revision J Always keep this manual with the instrument. Read carefully before working with the instrument. Version 1.3, Revision J - 01.2017 3 HistoCore SPECTRA ST The information, numerical data, notes and value judgments contained in this manual represent the current state of scientific knowledge and state-of-the-art technology as we understand it following thorough investigation in this field. We are under no obligation to update the present manual periodically and on an ongoing basis according to the latest technical developments, nor to provide our customers with additional copies, updates etc. of this manual. To the extent permitted in accordance with the national legal system as applicable in each individual case, we shall not be held liable for erroneous statements, drawings, technical illustrations etc. contained in this manual. In particular, no liability whatsoever is accepted for any financial loss or consequential damage caused by or related to compliance with statements or other information in this manual. Statements, drawings, illustrations and other information regarding the contents or technical details of the present Instructions for Use are not to be considered warranted characteristics of our products. These are determined only by the contract provisions agreed between ourselves and our customers. Leica reserves the right to change technical specifications as well as manufacturing processes without prior notice. Only in this way is it possible to continuously improve the technology and manufacturing techniques used in our products. This document is protected under copyright laws. All copyrights to this documentation are held by Leica Biosystems Nussloch GmbH. Any reproduction of text and illustrations (or of any parts thereof) by means of print, photocopy, microfiche, web cam or other methods – including any electronic systems and media – requires express prior permission in writing by Leica Biosystems Nussloch GmbH. For the instrument serial number and year of manufacture, please refer to the nameplate on the back of the instrument. Note Leica Biosystems Nussloch GmbH Heidelberger Str. 17 - 19 D-69226 Nussloch, Germany Germany Phone: +49 - (0) 6224 - 143 0 Fax: +49 - (0) 6224 - 143 268 Web: www.LeicaBiosystems.com 4 Version 1.3, Revision J Table of Contents 1. Important Information ................................................................................................................................8 1.1 Symbols and their meanings..........................................................................................................................8 1.2 Instrument type ..............................................................................................................................................12 1.3 User Group ......................................................................................................................................................12 1.4 Intended use ...................................................................................................................................................12 1.5 Copyright - Instrument software .................................................................................................................13 2. Security .......................................................................................................................................................14 2.1 Safety Notes ...................................................................................................................................................14 2.2 Warnings .........................................................................................................................................................15 2.3 Safety features on the instrument ..............................................................................................................18 3. Instrument Components and Specifications ........................................................................................19 3.1 Standard delivery ...........................................................................................................................................19 3.2 Specifications .................................................................................................................................................20 3.3 General overview - front view .....................................................................................................................22 3.4 General overview - rear view ......................................................................................................................23 3.5 General overview - inside view ...................................................................................................................24 4. Installation and Starting up ....................................................................................................................25 4.1 Installation site requirements ......................................................................................................................25 4.2 Rinsing water connection ............................................................................................................................25 4.2.1 Joint connection of all 6 rinsing water stations .......................................................................................26 4.2.2 Combined connection 4+2 rinsing water stations ....................................................................................27 4.2.3 Wastewater connection ...............................................................................................................................29 4.3 Electrical connection ......................................................................................................…

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RFID-Registration HistoCore SPECTRA ST RFID RFID RFID RFID-Registration HistoCore SPECTRA ST Order-No.: 14 0512 89998 RevB Always keep this information with the instrument. Read carefully before working with the instrument. V 1.1 RevB - 04/2016 1 For HistoCore SPECTRA ST RFID-Registration for Australia and New Zealand ............................................................................2 RFID-Registration for the Peoples Republic of China .......................................................................2 RFID-Registration for Israel ...................................................................................................................3 RFID-Registration for Japan ..................................................................................................................3 RFID-Registration for South Korea .......................................................................................................4 RFID-Registration for Singapore ...........................................................................................................5 RFID-Registration for the United Arab Emirates ................................................................................5 RFID-Registration for the United States of America and Canada ...................................................6 Table of Contents 2 RFID-Registration V 1.1 RevB – 04/2016 RFID-Registration HistoCore SPECTRA ST RFID-Registration for Australia and New Zealand Symbol on the Identification Label: Title of Symbol:RCM Compliance Mark Description: The Regulatory Compliance Mark (RCM) indicates a device's compliance with applicable ACMA technical standards of New Zealand and Australia – that is, for telecommunications, radio communications, EMC and EME. 3 For HistoCore SPECTRA ST RFID-Registration HistoCore SPECTRA ST הסמל על האריזה: MOCמספר רישום כותרת הסמל: מספר הרישום מציין שמכשיר אלחוטי קיבל אישור סוג במשרד התקשורת הישראלי. תיאור: RFID-Registration for Israel RFID-Registration for Japan 4 RFID-Registration V 1.1 RevB – 04/2016 RFID-Registration HistoCore SPECTRA ST 5 For HistoCore SPECTRA ST RFID-Registration HistoCore SPECTRA ST Symbol on the Identification Label: Title of Symbol:IDA compliance mark Description: Infocomm Development Authority (IDA) Type Approval is a requirement for Radio and Telecommunications Terminal Equipment (RTTE) to comply with specific technical specifications of Singapore. RFID-Registration for Singapore RFID-Registration for the United Arab Emirates 6 RFID-Registration V 1.1 RevB – 04/2016 RFID-Registration HistoCore SPECTRA ST Symbol on the Identification Label: FCC ID: 2AAPD-SPECTRAST IC: 12028A-SPECTRAST Title of Symbol:FCC-Approved Equipment Description: This device complies with Part 15 of the FCC Rules and with Industry Canada licence- exempt RSS standard(s). Operation is subject to the following two 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. Le présent appareil est conforme aux CNR d'Industrie Canada applicables aux ap- pareils radio exempts de licence. L'exploitation est autorisée aux deux conditions suivantes: (1) l'appareil ne doit pas produire de brouillage, et (2) l'utilisateur de l'appareil doit accepter tout brouillage radioélectrique subi, même si le brouillage est susceptible d'en compromettre le fonctionnement. RFID-Registration for the United States of America and Canada 7 For HistoCore SPECTRA ST RFID-Registration HistoCore SPECTRA ST RFID-Registration for the United States of America and Canada (Continued) This equipment has been tested and found to comply with the limits for a Class B digi- tal 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 ins- talled and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that 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. Changes or modifications made to this equipment not expressly approved by Leica Biosystems Nussloch GmbH may void the FCC authorization to operate this equip- ment. 8 RFID-Registration V 1.1 RevB – 04/2016 www.LeicaBiosystems.com Leica Biosystems Nussloch GmbH Heidelberger Straße 17-19 D- 69226 Nussloch Tel.: +49 - (0) 6224 - 143 0 Fax: +49 - (0) 6224 - 143 268 Web: www.LeicaBiosystems.com

Test report no.: 1-5922/13-17-01_AnnexA Page 1 of 5 Annex A This test report annex is electronically signed and valid without handwriting signature. For verification of the electronic signatures, the public keys can be requested at the testing laboratory. Test report annex authorised: Stefan Bös Professional Radio Communications & EMC Test report no.: 1-5922/13-17-01_AnnexA Page 2 of 5 External ph ot os o f t he EU T Photo 1: Photo 2: Test report no.: 1-5922/13-17-01_AnnexA Page 3 of 5 Photo 3: Photo 4: Test report no.: 1-5922/13-17-01_AnnexA Page 4 of 5 Photo 5: Photo 6: Test report no.: 1-5922/13-17-01_AnnexA Page 5 of 5 Docu men t his to r y Version Applied changes Date of release Initial release 2014-08-01

Test report no.: 1-5922/13-17-01_AnnexB Page 1 of 18 Annex B This test report annex is electronically signed and valid without handwriting signature. For verification of the electronic signatures, the public keys can be requested at the testing laboratory. Test report annex authorised: Stefan Bös Professional Radio Communications & EMC Test report no.: 1-5922/13-17-01_AnnexB Page 2 of 18 Inter nal p ho tos of the E UT Photo 1: Photo 2: Test report no.: 1-5922/13-17-01_AnnexB Page 3 of 18 Photo 3: Photo 4:13.56 MHz Reader Test report no.: 1-5922/13-17-01_AnnexB Page 4 of 18 Photo 5:13.56 MHz Reader Photo 6:125 kHz Reader (Drawer) Test report no.: 1-5922/13-17-01_AnnexB Page 5 of 18 Photo 7:125 kHz Reader (Drawer) Photo 8:125 kHz Reader (Drawer) Test report no.: 1-5922/13-17-01_AnnexB Page 6 of 18 Photo 9:125 kHz Reader (Drawer) Photo 10:125 kHz Reader (Drawer) Test report no.: 1-5922/13-17-01_AnnexB Page 7 of 18 Photo 11:125 kHz Reader (Drawer) Photo 12:125 kHz Reader (Drawer) Test report no.: 1-5922/13-17-01_AnnexB Page 8 of 18 Photo 13:125 kHz Reader (Drawer) Photo 14:125 kHz Reader (Drawer) Test report no.: 1-5922/13-17-01_AnnexB Page 9 of 18 Photo 15:125 kHz Reader (XYZ positioning system) Photo 16:125 kHz Reader (XYZ positioning system) Test report no.: 1-5922/13-17-01_AnnexB Page 10 of 18 Photo 17:125 kHz Reader (XYZ positioning system) Photo 18:125 kHz Reader (XYZ positioning system) Test report no.: 1-5922/13-17-01_AnnexB Page 11 of 18 Photo 19:125 kHz Reader (XYZ positioning system) Photo 20:125 kHz Reader (XYZ positioning system) Test report no.: 1-5922/13-17-01_AnnexB Page 12 of 18 Photo 21:125 kHz Reader (XYZ positioning system) Photo 22:125 kHz Reader (XYZ positioning system) Test report no.: 1-5922/13-17-01_AnnexB Page 13 of 18 Photo 23:125 kHz Reader (XYZ positioning system) Photo 24:125 kHz Reader (XYZ positioning system) Test report no.: 1-5922/13-17-01_AnnexB Page 14 of 18 Photo 25:125 kHz Reader (XYZ positioning system) Photo 26: 13.56 MHz Reader Test report no.: 1-5922/13-17-01_AnnexB Page 15 of 18 Photo 27:13.56 MHz Reader Photo 28:13.56 MHz Reader Test report no.: 1-5922/13-17-01_AnnexB Page 16 of 18 Photo 29:13.56 MHz Reader Photo 30:13.56 MHz Reader Test report no.: 1-5922/13-17-01_AnnexB Page 17 of 18 Photo 31:13.56 MHz Reader Photo 32:13.56 MHz Reader Test report no.: 1-5922/13-17-01_AnnexB Page 18 of 18 Docu men t his to r y Version Applied changes Date of release Initial release 2014-08-01

Page 1 of 25 TEST REPORT Test report no.: 1-5922/13-17-06 Testing laboratory Applicant CETECOM ICT Services GmbH Untertuerkheimer Strasse 6 – 10 66117 Saarbruecken / Germany Phone: + 49 681 5 98 - 0 Fax: + 49 681 5 98 - 9075 Internet: http://www.cetecom.com e-mail: [email protected] Accredited Testing Laboratory: The testing laboratory (area of testing) is accredited according to DIN EN ISO/IEC 17025 (2005) by the Deutsche Akkreditierungsstelle GmbH (DAkkS) The accreditation is valid for the scope of testing procedures as stated in the accreditation certificate with the registration number: D-PL-12076-01-00 Leica Biosystems Nussloch GmbH Heidelbergerstrasse 17-19 69226 Nussloch / GERMANY Phone: +49 62 24 14 30 Fax: +49-6224 143 5343 Contact: Marc Reiss e-mail: [email protected] Phone: +49-6224 143 343 Manufacturer Leica Biosystems Nussloch GmbH Heidelbergerstrasse 17-19 69226 Nussloch / GERMANY Test standard/s 47 CFR Part 15 Title 47 of the Code of Federal Regulations; Chapter I Part 15 - Radio frequency devices RSS - 210 Issue 8 Spectrum Management and Telecommunications - Radio Standards Specification Low-power Licence-exempt Radiocommunication Devices (All Frequency Bands): Category I Equipment For further applied test standards please refer to section 3 of this test report. Test Item Kind of test item: Multistainer Model name: HistoCore SPECTRA ST FCC ID: 2AAPD-SPECTRAST IC: 12028A-SPECTRAST Frequency: 13.56 MHz Technology tested: RFID Antenna: Integrated PCB loop antenna Power supply: 115V AC Temperature range: +18°C to +30°C This test report is electronically signed and valid without handwriting signature. For verification of the electronic signatures, the public keys can be requested at the testing laboratory. Test report authorised: Test performed: Marco Bertolino p.o. Stefan Bös Specialist Professional Radio Communications & EMC Radio Communications & EMC Test report no.: 1-5922/13-17-06 Page 2 of 25 1 Table of contents 1 Table of contents ............................................................................................................................................ 2 2 General information ....................................................................................................................................... 3 2.1 Notes and disclaimer .......................................................................................................................... 3 2.2 Application details ............................................................................................................................... 3 3 Test standard/s ............................................................................................................................................... 3 4 Test environment ............................................................................................................................................ 4 5 Test item .......................................................................................................................................................... 4 5.1 Additional information ........................................................................................................................ 4 6 Test laboratories sub-contracted ................................................................................................................. 4 7 Description of the test setup ......................................................................................................................... 5 7.1 Radiated measurements ..................................................................................................................... 5 7.2 Open area site ...................................................................................................................................... 6 7.3 AC conducted ...................................................................................................................................... 7 7.4 Conducted measurements ................................................................................................................. 8 8 Summary of measurement results ............................................................................................................... 9 9 Additional comments ................................................................................................................................... 10 10 Measurement results ............................................................................................................................ 11 10.1 Timing of the transmitter ............................................................................................................... 11 10.2 Field strength of the fundamental ................................................................................................ 13 10.3 99 % emission bandwidth ............................................................................................................. 14 10.4 Field strength of the harmonics and spurious ........................................................................... 15 10.5 Frequency tolerance ...................................................................................................................... 20 10.6 AC line conducted ......................................................................................................................... 21 11 Test equipment and ancillaries used for tests ................................................................................... 23 12 Observations ......................................................................................................................................... 23 Annex A Document history .......................................................................................................................... 24 Annex B Further information ......................................................................…

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Page 1 of 25 TEST REPORT Test report no.: 1-5922/13-17-05 Testing laboratory Applicant CETECOM ICT Services GmbH Untertuerkheimer Strasse 6 – 10 66117 Saarbruecken / Germany Phone: + 49 681 5 98 - 0 Fax: + 49 681 5 98 - 9075 Internet: http://www.cetecom.com e-mail: [email protected] Accredited Testing Laboratory: The testing laboratory (area of testing) is accredited according to DIN EN ISO/IEC 17025 (2005) by the Deutsche Akkreditierungsstelle GmbH (DAkkS) The accreditation is valid for the scope of testing procedures as stated in the accreditation certificate with the registration number: D-PL-12076-01-00 Leica Biosystems Nussloch GmbH Heidelbergerstrasse 17-19 69226 Nussloch / GERMANY Phone: +49 62 24 14 30 Fax: +49-6224 143 5343 Contact: Marc Reiss e-mail: [email protected] Phone: +49-6224 143 343 Manufacturer Leica Biosystems Nussloch GmbH Heidelbergerstrasse 17-19 69226 Nussloch / GERMANY Test standard/s 47 CFR Part 15 Title 47 of the Code of Federal Regulations; Chapter I Part 15 - Radio frequency devices RSS - 210 Issue 8 Spectrum Management and Telecommunications - Radio Standards Specification Low-power Licence-exempt Radiocommunication Devices (All Frequency Bands): Category I Equipment For further applied test standards please refer to section 3 of this test report. Test Item Kind of test item: Multistainer Model name: HistoCore SPECTRA ST FCC ID: 2AAPD-SPECTRAST IC: 12028A-SPECTRAST Frequency: 125 kHz Technology tested: RFID Antenna: Integrated loop antenna Power supply: 115V AC Temperature range: +18°C to +30°C This test report is electronically signed and valid without handwriting signature. For verification of the electronic signatures, the public keys can be requested at the testing laboratory. Test report authorised: Test performed: Marco Bertolino p.o. Stefan Bös Specialist Professional Radio Communications & EMC Radio Communications & EMC Test report no.: 1-5922/13-17-05 Page 2 of 25 1 Table of contents 1 Table of contents ............................................................................................................................................ 2 2 General information ....................................................................................................................................... 3 2.1 Notes and disclaimer .......................................................................................................................... 3 2.2 Application details ............................................................................................................................... 3 3 Test standard/s ............................................................................................................................................... 3 4 Test environment ............................................................................................................................................ 4 5 Test item .......................................................................................................................................................... 4 5.1 Additional information ........................................................................................................................ 4 6 Test laboratories sub-contracted ................................................................................................................. 4 7 Description of the test setup ......................................................................................................................... 5 7.1 Radiated measurements ..................................................................................................................... 5 7.2 Open area site ...................................................................................................................................... 6 7.3 AC conducted ...................................................................................................................................... 7 7.4 Conducted measurements ................................................................................................................. 8 8 Summary of measurement results ............................................................................................................... 9 8.1 Additional comments ........................................................................................................................ 10 9 Measurement results .................................................................................................................................... 11 9.1 Timing of the transmitter .................................................................................................................. 11 9.2 Bandwidth of the modulated carrier ................................................................................................ 13 9.3 Field strength of the fundamental ................................................................................................... 16 9.4 Fieldstrength of the harmonics and spurious ................................................................................ 17 9.5 Receiver spurious emissions ........................................................................................................... 20 9.6 Conducted limits ............................................................................................................................... 21 10 Test equipment and ancillaries used for tests ................................................................................... 23 11 Observations ......................................................................................................................................... 23 Annex A Document history .......................................................................................................................... 24 Annex B Further information ..........................................................................…

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Test report no.: 1-5922/13-17-01_AnnexE Page 1 of 6 Annex E This test report annex is electronically signed and valid without handwriting signature. For verification of the electronic signatures, the public keys can be requested at the testing laboratory. Test report annex authorised: Stefan Bös Professional Radio Communications & EMC Test report no.: 1-5922/13-17-01_AnnexE Page 2 of 6 EUT Test se tu p p h otos Photo 1: Photo 2: Test report no.: 1-5922/13-17-01_AnnexE Page 3 of 6 Photo 3: Photo 4: Test report no.: 1-5922/13-17-01_AnnexE Page 4 of 6 Photo 5: Photo 6: Test report no.: 1-5922/13-17-01_AnnexE Page 5 of 6 Photo 7: Test report no.: 1-5922/13-17-01_AnnexE Page 6 of 6 Docu men t his to r y Version Applied changes Date of release Initial release 2014-08-01