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S8Q-GN4215Endoscope Reprocessor with RFID

Olympus Medical Systems Corp.
Endoscope Reprocessor with RFID - FCC ID S8Q-GN4215 - Olympus Medical Systems Corp.
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Application Details

Equipment Class
DXX - Part 15 Low Power Communication Device Transmitter
Date of Grant
Nov 19, 2007
Application Purpose
Original Equipment
Date of Application
Nov 19, 2007
Equipment Note
Endoscope Reprocessor with RFID
Frequency Range
13.56000000 - 13.56000000
Company
Olympus Medical Systems Corp.
Country
Japan

Documents & Files

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Users Manual

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Attestation Statements

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Cover Letter(s)

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External Photos

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ID Label/Location Info

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Internal Photos

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Test Report

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Test Setup Photos

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Document Text

Text extracted from the exhibit documents filed with the FCC. Open a document above to read the original.

Users Manual

For details on installation and setup, refer to “Instructions - Installation Manual”. USA: CAUTION:Federal law restricts this device to sale by or on the order of a physician. INSTRUCTIONS ENDOSCOPE REPROCESSOR OER-Pro (For Aldahol III) Contents i ENDOSCOPE REPROCESSOR OER-Pro Operation Manual Contents Labels and Symbols ..................................................................... 1 Important Information — Please Read Before Use.................... 7 Intended use ............................................................................................. 7 Instruction manuals ................................................................................... 7 User qualifications ..................................................................................... 8 Ensuring the safety of reprocessing personnel ......................................... 8 Equipment compatibility ............................................................................ 10 Care and storage ...................................................................................... 10 Maintenance and administration ............................................................... 10 Repair and modification ............................................................................ 10 Disposal of waste fluids............................................................................. 11 Disposal of this equipment ........................................................................ 11 Signal words.............................................................................................. 11 Dangers, warnings, and cautions .............................................................. 12 Terms used in these manuals ................................................................... 14 Chapter 1Checking the Package Contents............................ 16 Chapter 2Nomenclature and Functions ................................. 20 2.1Front and top panel......................................................................... 20 2.2Rear panel ...................................................................................... 22 2.3Side panel ....................................................................................... 22 2.4Cleaning tub.................................................................................... 23 2.5Control panels ................................................................................. 24 2.6Consumable accessories (Optional) ............................................... 29 Chapter 3Inspection Before Use............................................. 32 3.1Inspecting for water leakage from the water supply piping and within the equipment ................................................................ 34 3.2Inspecting the equipment’s connectors........................................... 35 3.3Inspecting the connecting tubes and leak test air tube ................... 36 3.4Inspecting the remaining quantity of detergent, and replenishment 37 3.5Inspecting the remaining quantity of alcohol, and replenishment ... 43 3.6Inspecting the mesh filters .............................................................. 48 3.7Inspecting for disinfectant solution odor.......................................... 49 3.8Inspecting the disinfectant solution’s concentration level ............... 50 3.9Inspecting the printer paper roll ...................................................... 53 ii Contents ENDOSCOPE REPROCESSOR OER-Pro Operation Manual Chapter 4Basic Endoscope Reprocessing Operations ........ 54 4.1Power activation and opening the faucet ........................................ 57 4.2Inspection before use...................................................................... 60 4.3Endoscope precleaning .................................................................. 60 4.4Recognition of the Scope ID ........................................................... 61 4.5User ID detection ............................................................................ 64 4.6Endoscope setup ............................................................................ 66 4.7Leak test ......................................................................................... 72 4.8Connecting tube installation ............................................................ 78 4.9Reprocessing .................................................................................. 80 4.10 Alcohol flushing ............................................................................... 87 4.11 Removing the endoscopes ............................................................. 94 4.12 Printing of the reprocessing results................................................. 95 Chapter 5End-of-Day Checks.................................................. 109 5.1Turning the power OFF, closing the faucet and cleaning the outer surface ............................................................................. 110 5.2Cleaning the mesh filters................................................................. 111 5.3Removal or storage of alcohol ........................................................ 113 5.4Cleaning the fluid level sensor ........................................................ 116 Chapter 6Other Functions ....................................................... 119 6.1Confirming the disinfectant solution temperature............................ 119 6.2Heating the disinfectant solution ..................................................... 120 6.3Setting the reprocessing programs ................................................. 122 6.4Setting the disinfectant solution counter ......................................... 126 6.5Display of the total number of times the disinfectant solution was supplied........................................................................................... 131 6.6Display the total operation count of the equipment ......................... 131 6.7Air purge .....…

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Users Manual

52 Chapter 3 Inspection Before Use ENDOSCOPE REPROCESSOR OER-Pro Operation Manual 2.Push the drain connector into the disinfectant removal port until it clicks. When connecting the drain connector to the disinfectant removal port, do not push the connector’s head. Otherwise, disinfectant solution will leak out of it. 3.Place the prepared container below the drain connector, push the connector’s head, and collect the drained disinfectant solution until it is deep enough to immerse the reaction area of a test strip. Figure 3.20 4.While taking care not to inhale the disinfectant solution vapor, immerse the test strip in the disinfectant solution in the container to check the concentration. If the concentration is below the effective level, replace the disinfectant solution as described in Section 7.12, “Replacing the disinfectant solution” on page 176. 5.Place the prepared cloth under the drain connector, hold the lock lever and slowly disconnect the connector. Wipe off any disinfectant solution if it leaks. Aldahol III is indicated for use and reuse for the high-level disinfection of thoroughly cleaned, heat-sensitive medical equipment for 14 days or until the glutaraldehyde concentration decreases to 2.1%, whichever comes first. 6.Wipe the disinfectant removal port with a clean cloth and put the rubber cap back on. Rinse the disinfectant drain connector thoroughly in running water, dry it thoroughly and store in a clean place. 7.Close the front door. The front door cannot be closed unless the rubber cap is attached. Chapter 3 Inspection Before Use 53 ENDOSCOPE REPROCESSOR OER-Pro Operation Manual 3.9Inspecting the printer paper roll Do not start printing if the end of the printer paper roll is not projecting from the slit on the printer cover. Otherwise, the printer paper roll may jam and/or printing may fail. 1.Confirm that the end of the printer paper roll is projecting from the slit on the printer cover. If not, open the printer cover, unroll about 10 cm of paper and pass it through the slit. Figure 3.21 2.Close the printer cover and cut any excess paper projecting from the slit. Figure 3.22 54 Chapter 4 Basic Endoscope Reprocessing Operations ENDOSCOPE REPROCESSOR OER-Pro Operation Manual Chapter 4 Basic Endoscope Reprocessing Operations Before using this equipment for the first time or when it has not been used for a long period, full setup is required including installing accessories, connecting power and water supplies and disinfecting the equipment’s internal piping. Refer to Instructions-Installation Manual for details. Be sure to perform the preliminary checks before reprocessing scopes with this equipment and the post-operation checks afterwards. Otherwise, the equipment may not function at optimal levels. See Chapter 3, “Inspection Before Use” for details on the preliminary checks and Chapter 5, “End-of-Day Checks” for details on the final checks at the end of the day. Endoscopes must be precleaned before they are reprocessed with this equipment. Immediately after each examination, perform bedside cleaning, clean the outer surfaces, brush the forceps elevator areas and suction channel, and clean the valves, by referring to the cleaning, disinfection, and sterilization procedures described in the endoscopes’ instruction manuals. • When using the disinfectant solution and alcohol, Olympus recommends the use of gas filters and running this equipment in well-ventilated areas. Wear a facemask, gloves, and protective clothes to minimize aspiration and skin contact. Wear goggles for eye protection. Refer to the following association's guidelines related to ventilation: SGNA(Society of Gastroenterology Nurses and Associates) ASGE(American Society of Gastroenterological Endoscopy) APIC(Association for Professionals of Infection Control and Epidemiology) AORN(Association of Preoperative Registered Nurses) ASTM(American Society for Testing and Materials) OSHA(Occupational Safety and Health Administration) ACGIH(American Conference of Governmental Industrial Hygienists) Chapter 4 Basic Endoscope Reprocessing Operations 55 ENDOSCOPE REPROCESSOR OER-Pro Operation Manual • Always wear appropriate personal protective equipment, such as eye wear, face mask, moisture-resistant clothing, and chemical-resistant gloves that fit properly and are long enough so that your skin is not exposed. Otherwise, blood and mucus attached to the scopes could cause an infection. • All personal protective equipment should be inspected before use and replaced periodically before it is damaged. • Before cleaning and disinfecting an endoscope with this equipment, first connect the provided connector jigs to this equipment and then run through the cleaning and disinfecting process to disinfect the internal tubing. If the equipment is not properly disinfected, the endoscopes will not be properly reprocessed. • There is no data guaranteeing the sterilization effect of this equipment. Therefore, after cleaning/disinfecting an endoscope that requires sterilization, always be sure to sterilize the endoscope as instructed in its instruction manual. • Certain endoscopes cannot be reprocessed with this equipment. Refer to the provided “List of compatible Endoscopes/Connecting Tubes <OER-Pro>” to see which endoscopes are compatible. Do not attempt to reprocess an endoscope and its accessories that are not designated for use with the equipment or that are modified by a third party repair company; not only will the equipment be unable to function at optimal levels, the safety of the patient and operator may be endangered and this equipment and/or the endoscope may be damaged. Any repairs required as a result of reprocessing a non-designated endoscope will not be covered by the warranty, even if they occur before expiration of the warranty period. The following figure shows the general flow of reprocessing with this equipment. For reliable reprocessing, it is important to understand the cleaning and disinfection procedures tho…

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Users Manual

Chapter 5 End-of-Day Checks 109 ENDOSCOPE REPROCESSOR OER-Pro Operation Manual Chapter 5 End-of-Day Checks To ensure safe, reliable operation, inspect and clean all parts of the device regularly. • Be sure to inspect and clean the equipment as described in this chapter. Otherwise, the functions and performance of the equipment may not operate properly. • If any irregularity is observed, do not use the device and contact Olympus. If the device is used when an irregularity is observed, the device may malfunction. Water leakage, electric shock, burns, and/or fire may also result. • When inspecting the device, always wear appropriate personal protective equipment, such as eye wear, face mask, moisture-resistant clothing, and chemical-resistant gloves that fit properly and are long enough so that your skin is not exposed. All personal protective equipment should be inspected before use and replaced periodically before it is damaged. Check Checks at the end of every working day 5.1 Turning the power OFF, closing the faucet and cleaning the outer surface 5.2 Cleaning the mesh filters 5.3 Removal or storage of alcohol 5.4 Cleaning the fluid level sensor Table 5.1 Check Required items 70% ethyl alcohol or isopropyl alcohol Clean cloth Filter cleaning brush Table 5.2 110 Chapter 5 End-of-Day Checks ENDOSCOPE REPROCESSOR OER-Pro Operation Manual 5.1Turning the power OFF, closing the faucet and cleaning the outer surface • To prevent water leakage, be sure to close the water faucet at the end of the working day. • After using the device, dry it thoroughly (so that no water remains in the cleaning tub) and close the lid before storage. Otherwise, germs may penetrate the device and prevent effective reprocessing the next time the unit is used. • If the equipment has been stored after closing the lid without drying the cleaning tub completely, thoroughly wipe the inside of the cleaning tub with a cloth moistened with 70% ethyl alcohol or isopropyl alcohol before the next use. 1.Close the water faucet. 2.Press the power switch to OFF. 3.Using a clean cloth moistened with neutral detergent solution, clean every part of the device including the front and back of the lid, the lid packing, the edge and inside of the cleaning tub and the control panel, then wipe with a dry clean cloth. To prevent growth of various germs, it is also recommended to wipe every part of the equipment with a cloth moistened with 70% ethyl alcohol or isopropyl alcohol. Figure 5.1 Chapter 5 End-of-Day Checks 111 ENDOSCOPE REPROCESSOR OER-Pro Operation Manual 4.Step the foot pedal to open the lid, let the inside of the cleaning tub dry completely (so that no water remains in the tub), and close the lid. If the device has been stored after closing the lid without drying the cleaning tub completely, wipe the inside of the cleaning tub with a cloth moistened with 70% ethyl alcohol or isopropyl alcohol completely before the next use. 5.2Cleaning the mesh filters Clean the two circulation port mesh filters and the drain port mesh filter. Clogging a mesh filter not only impairs the operation of the device but may also cause a scope malfunction or prevent effective reprocessing. • If the mesh filters have been removed, be sure to put them back in their original positions before using the device. If you forget to attach the mesh filters, the pump may malfunction and/or foreign objects might get into the pipes or scope nozzles and clog them. • When cleaning the mesh filters, take care not to leave brush hair or cotton swab fiber in the meshes. Otherwise, their filtering effectiveness may be reduced. • If a mesh filter is dropped or subjected to an impact, make sure that the mesh shape is not deformed. Otherwise, the filtering effect may degrade. • Two mesh filters are installed on the outer and inner sides of the circulation port. Be sure to remove, inspect, and clean both of them. 112 Chapter 5 End-of-Day Checks ENDOSCOPE REPROCESSOR OER-Pro Operation Manual 1.Step the foot pedal to open the lid. 2.Remove the mesh filters from the cleaning tub. Figure 5.2 3.Clean each mesh filter in running water using a brush, cotton swab, etc. Figure 5.3 4.Attach the mesh filters in their original positions. Drain port mesh filter Circulation port mesh filters Chapter 5 End-of-Day Checks 113 ENDOSCOPE REPROCESSOR OER-Pro Operation Manual 5.3Removal or storage of alcohol If alcohol is left in the tank after work, a fire hazard may occur. Be sure to remove alcohol from the tank or take the tank out of the equipment and store it safely away from the device at the end of the working day. Before handling the alcohol, read the precautions carefully and use it as instructed. Do not tilt the alcohol tank while alcohol is inside. Otherwise, the alcohol may spill. Removing alcohol from the alcohol tank 1.Pull out the detergent/alcohol drawer. Figure 5.4 2.While pushing the lock lever on the connector of the tube connected to the cap of the alcohol tank. Figure 5.5 Cap Alcohol tank 114 Chapter 5 End-of-Day Checks ENDOSCOPE REPROCESSOR OER-Pro Operation Manual 3.Take the alcohol tank out of the device. 4.Turn the alcohol tank cap to remove it, discharge the alcohol from the tank and dry the inside. Figure 5.6 5.Attach the alcohol tank cap, place the alcohol tank in the detergent/alcohol drawer and connect the tube to the alcohol tank cap. Figure 5.7 6.Close the detergent/alcohol drawer. Cap Alcohol tank Chapter 5 End-of-Day Checks 115 ENDOSCOPE REPROCESSOR OER-Pro Operation Manual Storing alcohol tank outside the device Remove the alcohol in the alcohol tank and replace with new alcohol at least every week. Otherwise, the alcohol in the alcohol tank may degrade. 1.Pull out the detergent/alcohol drawer. Figure 5.8 2.While pushing the lock lever on the connector of the tube connected to cap of the alcohol tank, disconnect the tube. Figure 5.9 3.Take the alcohol tank out of the device. Cap Alcohol tank 116 Chapter 5 End-of-Day Checks ENDOSCOPE REPROCESSOR OER-Pro Opera…

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Users Manual

174 Chapter 7 Routine Maintenance ENDOSCOPE REPROCESSOR OER-Pro Operation Manual 2.Using a cloth moistened with neutral detergent solution, clean the external surfaces of the accessory holder and the accessories listed above, rinse them in running water, and wipe them with a clean cloth. To prevent the spread of various germs, it is also recommended to wipe the accessories and accessory holder with a cloth moistened with 70% ethyl alcohol or isopropyl alcohol. 3.Dry the accessories thoroughly and store them in a clean place near the device. 4.Attach the accessory holder to the back side of the front door using the two retaining screws. 5.Store the frequently used tubes in the accessory holder. Note that the accessory holder cannot accommodate all of the tubes. Figure 7.53 Do not hook tubes on the accessories holder in a disorderly fashion as this could make it impossible to open or close the front door and may also damage the accessories. Chapter 7 Routine Maintenance 175 ENDOSCOPE REPROCESSOR OER-Pro Operation Manual 7.11 Cleaning the alcohol tank Do not tilt the alcohol or detergent tank while fluid is still inside. Otherwise, the fluid may spill. 1.Pull out the detergent/alcohol drawer. 2.Disconnect the tube from the alcohol tank and take the tank out of the detergent/alcohol drawer. 3.Empty the tank. 4.Using a cloth moistened with neutral detergent solution, clean the external surface, rinse the inside and external surface of the tank in running water, and wipe it with a clean cloth. To prevent bacterial growth, wipe the outside of the tank with a cloth moistened with 70% ethyl alcohol or isopropyl alcohol. 5.Drain out the water inside the tank, dry it thoroughly, put it back on the detergent/alcohol drawer and attach the cap and tube to it. 6.Turn the connectors to correct the orientations of the tubes as shown below. Figure 7.54 7.Close the detergent/alcohol drawer. Connectors 176 Chapter 7 Routine Maintenance ENDOSCOPE REPROCESSOR OER-Pro Operation Manual 7.12 Replacing the disinfectant solution When the disinfectant solution in the device is no longer effective, drain the disinfectant solution completely and add new disinfectant solution. Waste fluid should be treated as directed in the documents supplied with Aldahol III. • Before handling the disinfectant solution, read the precautions carefully and use it as instructed. Be sure that you fully understand what measures need to be taken if you get any disinfectant solution on your skin. • When handling the disinfectant solution, wear appropriate personal protective equipment to prevent it from making direct contact with your skin and to prevent excessive inhalation of the vapor. The disinfectant solution and its vapor may adversely affect the human body. If you get disinfectant solution in your eyes, immediately rinse with a large quantity of water and then call the doctor. Personal protective equipment, such as eye wear, face mask, moisture-resistant clothing, and chemical-resistant gloves that fit properly and are long enough so that your skin is not exposed. All personal protective equipment should be inspected before use and replaced periodically before it is damaged. The disinfectant solution’s waste fluid should be treated in accordance with the instructions supplied with the Aldahol III. It is recommended to treat the waste fluid properly and to drain it according to local wastewater standards defined by law, or temporarily collect and store the waste fluid and have it treated by a waste disposal firm. Chapter 7 Routine Maintenance 177 ENDOSCOPE REPROCESSOR OER-Pro Operation Manual Draining the disinfectant solution Before draining the disinfectant solution, disconnect the connecting tube from the connector on the device. Otherwise, the disinfectant solution may spout out of the tube, causing a leak from the cleaning tub. Draining through the disinfectant collection hose • Do not block the disinfectant removal port with a finger when the rubber cap is not attached. Otherwise, the disinfectant solution may flow out. • To prevent the device and facilities near the equipment from being damaged by leaked disinfectant solution, do not remove the rubber cap from the disinfectant removal port except when the disinfectant removal tube is connected. • If disinfectant solution leaks out of the disinfectant removal port when the rubber cap has been removed, immediately reattach the rubber cap and follow the procedure in Section 8.1, “Troubleshooting guide” on page 218. If it does not stop leaking, contact Olympus. Drained disinfectant solution Drain quantityApproximately 17.5 L (4.6 gallons) Table 7.12 Check Required items Disinfectant collection hose Disinfectant removal tube Containers (Large) with 18 L (5 gallons) or larger capacity such as PVC tanks (u2) Container (Small) with 200 mL or larger capacity (wide-mouthed container such as a vat) Clean cloth Table 7.13 178 Chapter 7 Routine Maintenance ENDOSCOPE REPROCESSOR OER-Pro Operation Manual • When handling the disinfectant solution, wear appropriate personal protective equipment to prevent it from making direct contact with your skin and to prevent excessive inhalation of the vapor. The disinfectant solution and its vapor may adversely affect the human body. If you get disinfectant solution in your eyes, immediately rinse with a large quantity of water and then call the doctor. Personal protective equipment, such as eye wear, face mask, moisture-resistant clothing, and chemical-resistant gloves that fit properly and are long enough so that your skin is not exposed. All personal protective equipment should be inspected before use and replaced periodically before it is damaged. • Be sure to disconnect the disinfectant collection hose after collecting the disinfectant solution. If the device is run with the disinfectant collection hose connected, the cleaning fluid and disinfectant solution may leak out of the device. • Be sure to disconnect the drain connector except when collec…

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External Photos

Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 1 of 5 Version 0.1 External Photographs (OER-Pro) Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 2 of 5 Version 0.1 Front Rear Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 3 of 5 Version 0.1 Left Right Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 4 of 5 Version 0.1 To p Front Panel Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 5 of 5 Version 0.1 Operation Panel RFID Antenna

ID Label/Location Info

For US Figure 3 shows an overall view of the “Affix FCC Label” of figure 1 and figure2 in the precedent page. For Canada Figure 3 shows an overall view of the “Affix IC Label” of figure 1 and figure 2 in the precedent page. 120mm 70mm Figure 3.FCC and IC Label

Internal Photos

Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 1 of 8 Version 0.1 Internal Photographs (OER-Pro) Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 2 of 8 Version 0.1 Front Rear Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 3 of 8 Version 0.1 Left Right Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 4 of 8 Version 0.1 RFID Module (Left Side) Module : R/W Unit & I/F Unit Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 5 of 8 Version 0.1 Module : Antenna Unit RFID Antenna Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 6 of 8 Version 0.1 Module (R/W Unit) : Top Module (R/W Unit) : Bottom Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 7 of 8 Version 0.1 Module (I/F Unit) : Top Module (I/F Unit ) : Bottom Report No. ESJ–107088 FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 8 of 8 Version 0.1 Antenna Unit & R/W Unit Scope ID master card & RFID Antenna

Test Report

Report No. ESJñ107088A FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 1 of 23 Version 0.1 TEST REPORT Regulation : FCC Part15 Subpart C Section 15.225 Industry Canada RSS-210 Issue 7 Industry Canada RSS-Gen Issue 2 Applicant Testing Laboratory OLYMPUS MEDICAL SYSTEMS CORP. 2951 Ishikawa-cho Hachioji-shi, Tokyo 192-8507 Japan Tel : +81 3 426 42 2891 Fax : +81 3 426 42 3174 ETL SEMKO Japan K.K. Kashima Site 3-2 Sunayama, Kamisu, Ibaraki 314-0255 Japan Tel.: +81 479 40 1097 Fax.: +81 479 46 1788 URL: http://www.japan.intertek-etlsemko.com Equipment Type ENDOSCOPE REPROCESSOR Category Medical Equipment Trademark OLYMPUS Model (s) OER-Pro Serial No. 2700250 FCC ID S8Q-GN4215 IC 4763B-GN4215 Test Result Complied Report Number ESJ-107088A Report Issue Date November 20, 2007 This equipment has been shown to be capable of compliance with the applicable standard(s) as indicated in the test report. I attest to the accuracy of data. All measurements reported herein were performed by me or were made under my supervision and are correct to the best of my knowledge and belief. I assume full responsibility for the completeness of these measurements and vouch for the qualifications of all persons taking them. This test report shall not be reproduced partially, or in full, without the prior written approval of ETL SEMKO Japan K.K. The results and statements contained in this report pertain only to the equipment evaluated. As for this report, it is the test report issued again instead of ESJ-107088. Approved by Tested by Junichi Okada [ Site Manager ] Kazuo Masuda Naoki Ikeda Report No. ESJñ107088A FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 2 of 23 Version 0.1 TABLE OF CONTENTS Page SECTION 1. GENERAL INFORMATION ........................................................................................................... 3 SECTION 2. SUMMARY OF TEST RESULTS ...................................................................................................4 SECTION 3. INFORMATION ABOUT EUT ....................................................................................................... 5 SECTION 4. SUPPORT EQUIPMENT(S) ............................................................................................................ 6 SECTION 5. USED CABLE (S)............................................................................................................................ 7 SECTION 6. CONSTRUCTION OF EQUIPMENT ............................................................................................. 8 SECTION 7. OPERATING CONDITION........................................................................................................... 10 SECTION 8. TEST PROCEDURE(S) ................................................................................................................. 11 SECTION 9. EVALUATION OF TEST RESULTS............................................................................................. 15 SECTION 10. LIST OF MEASURING INSTRUMENTS .................................................................................... 21 SECTION 11. MEASUREMENT UNCERTAINTY ............................................................................................. 22 SECTION 12. DESCRIPTION OF TEST LABORATORY .................................................................................. 23 Report No. ESJñ107088A FCC ID : S8Q-GN4215 / IC : 4763B-GN4215 © ETL SEMKO Japan K.K. Page 3 of 23 Version 0.1 SECTION 1. GENERAL INFORMATION TEST PERFORMED Location Kashima No.3 Test Site (FCC Reg. : JP5026) (IC File No. : IC 2065A-3 ) EUT Received February 20, 2007 Te s t St a r t e d February 20, 2007 Te s t C o m p l e t e d May 2, 2007 Standard Applied FCC Part15C ñ Section 15.225 Industry Canada RSS-210 Issue 7 Industry Canada RSS-Gen Issue 2 Test Setup ANSI C63.4-2003 Deviation from Standard (s) No deviation TEST …

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Contact Information

Applicant

Yoshio Fukuda
[email protected]81426422111Fax: 81426422111

Technical Contact

PCTEST Engineering Laboratory, Inc.Randy Ortanez
[email protected]410-290-6652

6660-B Dobbin Road · Columbia, Maryland · United States

Test Firm

Intertek Japan K.K. Kashima SiteTakeshi Yamanaka
[email protected]81-479-40-1097Fax: 81-479-46-1788

Technical Specifications

#Rule PartsFrequency RangePower OutputTolerance
115C13.56 MHz - 13.56 MHz-0.0100000000 %
Confidentiality
Long Term

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