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QRICM06-1Patient Device

BIOTRONIK SE & Co. KG
Patient Device - FCC ID QRICM06-1 - BIOTRONIK SE & Co. KG
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Application Details

Equipment Class
PCT - PCS Licensed Transmitter worn on body
Date of Grant
Jul 26, 2006
Application Purpose
Original Equipment
Date of Application
Jul 12, 2006
Equipment Note
Patient Device
Frequency Range
824.20000000 - 848.80000000
Company
BIOTRONIK SE & Co. KG
Country
Germany

Documents & Files

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Users Manual

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Cover Letter(s)

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External Photos

ID Label/Location Info

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Internal Photos

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Operational Description

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RF Exposure Info

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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

CardioMessenger II ® Transmitter for BIOTRONIK Home Monitoring ® sbiotronik Technical Manual 356845_Cover_CMII_US.qxd 10.05.06 13:45 Seite 1 Overview Physician callback signal . . . . . . . . . . .Follow-up data transmission . . . . . . . .Ready (CardioMessenger II) . . . . . . . . .Battery monitor light . . . . . . . . . . . . . . .Ready (charging station) . . . . . . . . . . . .Data interface A view of the rear side of the device can befound on the back cover. 356845_Cover_CMII_US.qxd 10.05.06 13:45 Seite 2 Overview On/off buttonRestartPower supply portTelephone jackBelt clip 356845_Cover_CMII_US.qxd 10.05.06 13:45 Seite 3 BIOTRONIK GmbH & Co. KGWoermannkehre 112359 Berlin · GermanyTel +49 (0) 30 68905-0Fax +49 (0) 30 6852804BIOTRONIK, Inc.6024 SW Jean rd. Bldg. BLake Oswego, OR 97035Phone (800) 547-0394 (24-hr)Fax (503) 635-9936sales @ biotronik.com www.biotronik.com © by BIOTRONIK GmbH & Co. KG All rights reserved. Specifications subject to modification, revisionand improvement. ® CardioMessenger is a r egistered trademark of BIOTRONIK GmbH & Co. KG sbiotronik 356845/A/6D20 356845_Cover_CMII_US.qxd 10.05.06 13:45 Seite 4 1 ContentsWhat is Home Monitoring? . . . . . . . . . . . . 3Included Equipment . . . . . . . . . . . . . . . . . . 4How Do I Use the CardioMessenger? . . . . 6Where Should I Put the CardioMessenger? 6How Do I Install the CardioMessenger? . . 9 Telephone Connection . . . . . . . . . . . . . 12 Version A . . . . . . . . . . . . . . . . . . . . . . . . 13 Version B . . . . . . . . . . . . . . . . . . . . . . . . 19 How Do I Understand the Lights of the CardioMessenger? . . . . . . . . . . . . . . . . . . 25 Light 1 . . . . . . . . . . . . . . . . . . . . . . . . . . 25 Light 2 . . . . . . . . . . . . . . . . . . . . . . . . . . 26 Light 3 . . . . . . . . . . . . . . . . . . . . . . . . . . 26 Light 4 . . . . . . . . . . . . . . . . . . . . . . . . . . 27 Light 5 . . . . . . . . . . . . . . . . . . . . . . . . . . 28 How Do I Turn On the CardioMessenger? 29How Do I Turn Off th e CardioMessenger? 30 How Do I Charge the CardioMessenger? . 31How Do I Resolve Problems? . . . . . . . . . . 32 Light 3 . . . . . . . . . . . . . . . . . . . . . . . . . . 32 Light 4 . . . . . . . . . . . . . . . . . . . . . . . . . . 33 Light 5 . . . . . . . . . . . . . . . . . . . . . . . . . . 33 How Do I Reset the CardioMessenger? . . 34How Do I Take Care of the CardioMessenger? . . . . . . . . . . . . . . . . . . . 35 How Do I Carry the CardioMessenger? . . 36Safety Precautions - What Should I Watch Out For? . . . . . . . . . . . . . . . . . . . . . . . . . . . 38Guidelines . . . . . . . . . . . . . . . . . . . . . . . . . . 40USA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40 Canada . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41 Electromagnetic Compatibility . . . . . . . . . 42Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . 43 CardioMessenger.book Page 1 Tuesday, May 2, 2006 5:05 PM 2 Technical Data . . . . . . . . . . . . . . . . . . . . . . 44General . . . . . . . . . . . . . . . . . . . . . . . . . . . 44 Permissible Environmental Conditions . . 44 During Operation: . . . . . . . . . . . . . . . . . 44 Shipping and Storage: . . . . . . . . . . . . . 44 CardioMessenger Remote Unit . . . . . . . . 44CardioMessenger Charging Station . . . . 45Rechargeable Battery (integrated) . . . . . 45Power Supply . . . . . . . . . . . . . . . . . . . . . . . 45 Appendix . . . . . . . . . . . . . . . . . . . . . . . . . . 46 CardioMessenger.book Page 2 Tuesday, May 2, 2006 5:05 PM 3 What is Home Monitoring?Dear Patient:You have received a BIOTRONIK pacemaker or implantable cardioverter-defibrillator (ICD) with Home Monitoring function. Home Monitoring pacemakers and ICDs are additionally equipped with a special transmitter. This transmitter automatically transmits medical and technical information to a mobile device, the CardioMessenger. The CardioMessenger works like a cell phone and automatically transmits the information received from your implant as encoded messages to the BIOTRONIK Service Center.The transmission power from your implant is low so as to not impair your health in any way. Since the transmis sion range is short, the CardioMessenger is needed to send the information to the BIOTRONIK Service Center.At the Service Center, the data are processed and can be viewed only by your physician on a secured Internet site in the form of a comprehensive report called a Cardio Report. Your doctor can use this Cardio Report to decide whether your implant settings need to be updated or if your therapy plan needs to be changed. Thus, Home Monitoring serves as a practical diagnostic aid. CardioMessenger.book Page 3 Tuesday, May 2, 2006 5:05 PM 4 Included EquipmentThe set comes equipped with the following components:1. Mobile unit2. Charging station3. Power supply unit4. Power supply cable5. Belt clip (already affixed)6. Carrying strap7. Patient manual8. Telephone cable CardioMessenger.book Page 4 Tuesday, May 2, 2006 5:05 PM 5 Before use, make sure that none of the components are visibly damaged and that all necessary components have been delivered to you. Caution! Never use the CardioMessenger if it has been damaged; return it to your physician. Only use the following original BIOTRONIK devices, as other accessories can increase the interference emitted and the device's susceptibility to interference:- The CardioMessenger- The charging station with the appropriate power supply unit (type: FW 7555 M/06)- The power cord (type: BIOTRONIK NK-29, NK-30, or NK-31) - The telephone cord (type: BIOTRONIK VK-117) CardioMessenger.book Page 5 Tuesday, May 2, 2006 5:05 PM 6 How Do I Use the CardioMessenger?The following section describes: 2 How to optimize CardioMessenger placement 2 How to operate it 2 How it functions Where Should I Put the CardioMessenger?On your bedside table or close to your bed is a suitable place for your CardioMessenger since it generally fulfills …

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Users Manual

15 Take the telephone cable that came with the CardioMessenger, remove the second safety plug from the charging station and plug one end of the telephone cable into the port. CardioMessenger.book Page 15 Tuesday, May 2, 2006 5:05 PM 16 Insert the other end of your telephone cable into the telephone socket in your wall. CardioMessenger.book Page 16 Tuesday, May 2, 2006 5:05 PM 17 Now, place the CardioMessenger into the charging station. The CardioMessenger should switch itself on immediately, unless the batteries are completely depleted. A brief tone will sound when the CardioMessenger is switched on. If the batteries are completely depleted, then the CardioMessenger first charges itself and then switches itself on later (approximately after 30 minutes). Additional information can be found in „Version B" on page 19. CardioMessenger.book Page 17 Tuesday, May 2, 2006 5:05 PM 18 When you are finished, the connection should look like as follows: CardioMessenger.book Page 18 Tuesday, May 2, 2006 5:05 PM 19 Version BIf you wish to set up the CardioMessenger close to a telephone outlet, but there is no telephone, you may connect the CardioMessenger directly to the telephone outlet. Please proceed as follows:Take the telephone cable that came with the CardioMessenger and remove the safety plug on port 1 on the rear side of the charging station. CardioMessenger.book Page 19 Tuesday, May 2, 2006 5:05 PM 20 Now insert one end of your telephone cable into the port of the charging station. CardioMessenger.book Page 20 Tuesday, May 2, 2006 5:05 PM 21 Insert the other end of your telephone cable into the telephone socket in your wall. CardioMessenger.book Page 21 Tuesday, May 2, 2006 5:05 PM 22 Now, place the CardioMessenger in the charging station. The CardioMessenger should switch itself on immediately, unless the batteries are completely depleted. A brief tone will sound when the CardioMessenger is switched on. If the batteries are depleted, then the CardioMessenger first charges itself and then switches itself on later (approximately after 30 minutes). Additional information can be found in „Version B" on page 18. CardioMessenger.book Page 22 Tuesday, May 2, 2006 5:05 PM

Users Manual

23 When you are finished, the connection should look like as follows: CardioMessenger.book Page 23 Tuesday, May 2, 2006 5:05 PM 24 CardioMessenger.book Page 24 Tuesday, May 2, 2006 5:05 PM 25 How Do I Understand the Lights of the CardioMessenger?Your CardioMessenger has four lights and one light on the ch arging station. The lights numbered 1 - 3 represent the general functions of the CardioMessenger, light 4 is the battery mo nitor light, and light 5 shows the operational status of the charging station.Note: Whether or not the li ghts flash or are lit continuously, the operation of your implant remains unaffected. Light 1 Off – This is the normal status. Yellow flashing – When this light flashes yellow, your physician wa nts you to call. This situation may never occur. You will be informed by your physician if s/he will use this feature. CardioMessenger.book Page 25 Tuesday, May 2, 2006 5:05 PM 26 Note: After you have switched the CardioMessenger off and on, this light will not flash anymor e. However, please do not forget to call your physician. Light 2 This light will only be used during a follow- up visit and can be triggered via the implant programmer ICS 3000. Your physician will find further information in the ICS 3000 manual.Note: Light 2 is not illuminated when your implant transmits regular messages. This light may be illumi nated or flash yellow, or flash green. Off – This is the normal status. Yellow illumination – When the light is illuminated yellow, the CardioMessenger is receiving a message. Please wait until the data transmission has finished (light flashing green) before yo u walk away from the CardioMessenger. Green flashing – When the light flashes green several times, the transmission of the message has been completed.Yellow flashing – However, when the light flashes yellow several times, the transmission was not successful. Your physician will decide what to do next. Light 3 This light informs you about the normal operation of the CardioMessenger. Green flashing – When the light sing le-flashes green repeatedly, the CardioMessenger is operating properly. This is the normal status. CardioMessenger.book Page 26 Tuesday, May 2, 2006 5:05 PM 27 Green flashing – When the light double-flashes green repeatedly, the CardioMessenger is also operating properly. Additionally, there are messages stored that have to be transmitted to the Service Center.Yellow flashing – When the light doubl e-flashes yellow repeatedly, there is no connection to the GSM network or modem and additionally the CardioMessenger has messages stored to be transmitted to the Service Center. For further information, see the „How Do I Resolve Problems?" on page 32. Yellow illumination – When the light is illuminated yellow, the CardioMessenger is performing a self-test. This test should last no longer than 10 seconds after the CardioMessenger has been switched on. Off – The CardioMessenger is switched off. Light 4 In the following, the four statuses of the battery monitor light are described as follows:Green Illumination – When the light is illuminated green, the CardioMessenger is fully charged. You may now use it in mobile operation for at least 24 hours. But the CardioMessenger can certainly also be kept in the charging station. Off – This is the normal status when the CardioMessenger is used in mobile operation.When this light is off but the CardioMes-senger is in the char ging station, please refer to „How Do I Resolve Problems?" on page 32. CardioMessenger.book Page 27 Tuesday, May 2, 2006 5:05 PM 28 Red flashing – When the light flashes red, the CardioMessenger batteries are nearly depleted. Please place the CardioMessenger in the charging station.Yellow illumination – When the light is illuminated yellow, the CardioMessenger is charging. Light 5 Green Illumination – This is the normal status when the charging station is connected to the power supply. If this is not the ca se, there might be an error. Additional information can be found in „How Do I Resolve Problems?" on page 32. CardioMessenger.book Page 28 Tuesday, May 2, 2006 5:05 PM 29 How Do I Turn On the CardioMessenger?As soon as you place the CardioMessenger in the charging station, it is automatically switched on. You certainly may also switch on the CardioMessenger when it is not placed in the charging station; the On/Off button is located on the right side of the CardioMessenger.Press the On/Off button of the CardioMessenger until you can feel slight resistance. A brief tone will sound, the CardioMessenger will start its self-test, and light 3 will be illuminated yellow. You can now release the button. CardioMessenger.book Page 29 Tuesday, May 2, 2006 5:05 PM 30 When the self-test of the CardioMessenger has finished, light 3 flashes yellow. Now, the CardioMessenger will try to connect to the BIOTRONIK Service Center.After a successful connection to the Service Center, light 3 flashes green. Your CardioMessenger is now operational. In case light 3 does not flash green, please refer to „How Do I Resolve Problems?" on page 32. Note: When the CardioMessenger has not been used for a long time or if it was stored below operational temperature, the battery can be completely depleted. In this case, the CardioMessenger switches itself on only after the battery has been charged for about 30 minutes. How Do I Turn Off the CardioMessenger?Press and hold the CardioMessenger On/Off button for at least two seconds. A brief tone will sound and light 3 wi ll go out after a short period of time.The CardioMessenger is switched off; no data can be received or transmitted.Note: A switched-off or improperly functioning CardioMessenger does not affect the operation of your implant. CardioMessenger.book Page 30 Tuesday, May 2, 2006 5:05 PM 31 How Do I Charge the CardioMessenger?The CardioMessenger has to be charged when the battery moni tor light (light 4) flashes red. If you wish to use the CardioMessenger in mobile operation, you should charge it every 24 hour…

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ID Label/Location Info

BIOTRONIK Telefon (+49 30) 689 05-0 Geschäftsführer: Kommanditgesellschaft: Meß- und Therapiegeräte Telefax (+49 30) 689 05-655 Dr. Max Schaldach HRA 6501, AG Berlin-Charlottenburg GmbH & Co KG. E-mail: [email protected] Christoph Böhmer Komplementärin: BIOTRONIK GmbH Woermannkehre 1 www.biotronik.de Dr. Lothar Krings HRB 2918, AG Berlin-Charlottenburg D-12359 Berlin Dr. Werner Braun BIOTRONIK GmbH & Co KG. • Postfach 47 02 55 • 12311 Berlin, Germany Federal Communications Commission Equipment Authorization Branch 7435 Oakland Mills Road Columbia, MD 21046 Berlin, 2006-03-29 Re: Label Location Information FCC ID: QRICM06-1

ID Label/Location Info

BIOTRONIK GmbH & Co. KGTelefon (+49 30) 689 05-0Geschäftsführer:Kommanditgesellschaft: Woermannkehre 1Telefax (+49 30) 689 05-1921Dr. Max SchaldachHRA 6501, AG Berlin-Charlottenburg D-12359 BerlinE-mail: [email protected] BöhmerKomplementärin: BIOTRONIK Meß- Steuer-Nr.: 30/062/05167www.biotronik.deDr. Werner Braun und Therapiegeräte GmbH USt.-Ident Nr.: 136651322Dr. Lothar KringsHRB 2918, AG Berlin-Charlottenburg BIOTRONIK GmbH & Co. KG • Postfach 47 02 55 • 12311 Berlin Federal Communications Commission Equipment Authorization Branch 7435 Oakland Mills Road Columbia, MD 21046 USA Berlin, April 7, 2006 Re: Label Sample FCC ID: QRI CM06-1

Internal Photos

ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 6 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 7 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 8 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 9 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 10 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 11 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 12 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 17 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 18 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 19 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 20 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 21 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 22 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 23 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 24 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 25 of 30 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-P-2224 Page 26 of 30

Operational Description

Applicant: Biotronik GmbH QRICM06-1 Telex3 GSM/PCS Antenna Specification S11 Quadbandantenna V2 Biotronik Feb.08.2006 -20 -18 -16 -14 -12 -10 -8 -6 -4 -2 0 500 750 1000 1250 1500 1750 2000 2250 2500 f/MHz magS11/dB Mobile in charging station Mobile free GSM 850/900GSM 1800/1900 Fig 1: Return loss Fig 2: Outlines, Dimensions in μm Applicant: Biotronik GmbH QRICM06-1 Biotronik Dev1 Channel: 128 peak EIRP [dBm]: 30.38 TRP [dBm]: 27.97 xy- plane xz- planeyz- plane 0 30 60 90 120 150 180 210 300 330 y 30 20 10 0 240 270 x Ф-Diagr. E Total 90 60 30 0 -30 -60 -90 -120 150 120 z 30 20 10 0 -150 180 x Θ-Diagr. E Total 90 60 30 0 -30 -60 -90 -120 150 120 z E Total 30 20 10 0 -150 180 y Θ-Diagr. x z y φ φφ φ θ θθ θAntenna Display Figure 3: Polar diagrams GSM850 Channel: 128 Biotronik Dev1 Channel:661 peak EIRP [dBm]:29.54 TRP [dBm]:25.14 xy- plane xz- planeyz- plane 0 30 60 90 120 150 180 210 300 330 y 30 20 10 0 240 270 x Ф-Diagr. E Total 90 60 30 0 -30 -60 -90 -120 150 120 z 30 20 10 0 -150 180 x Θ-Diagr. E Total 90 60 30 0 -30 -60 -90 -120 150 120 z E Total 30 20 10 0 -150 180 y Θ-Diagr. x z y φ φφ φ θ θθ θAntenna Display Figure 4: Polar diagrams GSM1900 Channel: 661

Operational Description

ZONEREVDESCRIPTIONDATEAPPROVED LINX TECHNOLOGIES 575 S.E.Ashley, Pl. Grants Pass, OR 97526 PHONE:541-471-6256 FAX:541-471-6251 www.linxtechnologies.com SIZE A FSCM NO.DWG NO. DESIGN: DRAWING: APPROVED: SERIES NUMBER STATUS:DRAFT/APPROVED DATE:__2_/__15_/___99__ PATH PARTNUMBER SHEET SCALE TITLE A/D CG LP ANT-***-LP LP Series Antaenna Specs

RF Exposure Info

___________________________________________________________________________________________________ -ETS- DR. GENZ GMBH STORKOWER STRASSE 38c,D-15526 REICHENWALDE B. BERLIN TELEPHONE +49-33631-888 00 TELEFAX +49-33631-888 660 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ELECTRONIC TECHNOLOGY SYSTEMS DR. GENZ GMBH - ETS - STORKOWER STRASSE 38c, D-15526 REICHENWALDE B. BERLIN Tel: 033631 888 00 FAX: 033631 888 660 D2: 900MHz SYSTEM VALIDATION DIPOLE C C C A A A L L L I I I B B B R R R A A A T T T I I I O O O N N N C C C E E E R R R T T T I I I F F F I I I C C C A A A T T T E E E 900 MHz System Validation Dipole (Muscle) Type: D900V2 Serial Number: 164 Place of Calibration: Reichenwalde Date of Calibration:September 05, 2003 Calibration Interval: 24 month ETS Dr. Genz GmbH hereby certifies, that this device has been calibrated on the date indicated above. The calibration was performed in accordance with specifications and procedures of ETS Dr. Genz GmbH. Wherever applicable, the standards used in the calibration process are traceable to International standards. Calibrated by: W. Treffke Approved by: K. Damm ___________________________________________________________________________________________________ -ETS- DR. GENZ GMBH STORKOWER STRASSE 38c,D-15526 REICHENWALDE B. BERLIN TELEPHONE +49-33631-888 00 TELEFAX +49-33631-888 660 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ELECTRONIC TECHNOLOGY SYSTEMS DR. GENZ GMBH - ETS - STORKOWER STRASSE 38c, D-15526 REICHENWALDE B. BERLIN Tel: 033631 888 00 FAX: 033631 888 660 D D D A A A S S S Y Y Y DIPOLE VALIDATION KIT Type:D900V2 Serial:164 Manufactured :April 30, 2002 Calibrated:September 05, 2003 ___________________________________________________________________________________________________ -ETS- DR. GENZ GMBH STORKOWER STRASSE 38c,D-15526 REICHENWALDE B. BERLIN TELEPHONE +49-33631-888 00 TELEFAX +49-33631-888 660 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH Measurement Conditions The measurements were performed in the flat section of the new SAM twin phantom filled with body simulating solution of the following electrical parameters at 900 MHz: Relative permittivity54.41+/- 5 % Conductivity1.038 mho/m +/- 10 % The DASY System with a dosimetric E-field probe ET3DV6 (SN: 1711, conversion factor 6.2 at 900 MHz body) was used for the measurements. The dipole feed-point was positioned below the center marking and oriented parallel to the body axis (the long side of the phantom). The standard measuring distance was 10 mm from dipole center to the solution surface. The included distance holder was used during measurements for accurate distance positioning. The coarse grid with a grid spacing of 5 mm was aligned with the dipole. The 7x7x7 fine cube was chosen for cube integration. The dipole input power (forward power) was 250 mW +/- 3 %. The results are normalized to 1 W input power. ___________________________________________________________________________________________________ -ETS- DR. GENZ GMBH STORKOWER STRASSE 38c,D-15526 REICHENWALDE B. BERLIN TELEPHONE +49-33631-888 00 TELEFAX +49-33631-888 660 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH SAR Measurement with DASY4 System Standard SAR-measurements were performed according to the measurement conditions described in section 4. The results (see figure supplied) have been normalized to a dipole input power of 1 W (forward power). The resulting averaged SAR-values measured with the dosimetric probe ET3DV6 SN:1711 and applying the advanced extrapolation are: Averaged over 1 cm3 (1 g) of tissue:11.2 mW/g Averaged over 10 cm3 (10 g) of tissue:7.16 mW/g Dipole impedance and return loss The dipole was positioned at the flat phantom sections according to section 4 (Measurement conditions) (with body tissue inside the phantom) and the distance holder was in place during impedance measurements. Feed-point impedance at 900 MHz: Re {Z} = 54.3 Ω Im {Z} = -3.2 Ω Return Loss at 900 MHz: - 23.6 dB Date/Time: 09/05/03 13:33:02 Test Laboratory: ELECTRONIC TECHNOLOGY SYSTEMS DR. GENZ GMBH File Name: Dipol Calibr.900 (m) 250mW.da4 Dipol Calibr.900 (m) 250mW DUT: Dipole 900 MHz; Type: D900V2; Serial: SN: 164 Program: Dipol Calibration 900 Muscle Communication System: CW; Frequency: 900 MHz;Duty Cycle: 1:1 Medium: Muscle 900 MHz (σ = 1.03749 mho/m, ε r = 54.4094, ρ = 1000 kg/m 3 ) Phantom section: Flat Section DASY4 Configuration: z Probe: ET3DV6 - SN1711; ConvF(6.2, 6.2, 6.2); Calibrated: 11/29/2002 z Sensor-Surface: 4mm (Mechanical And Optical Surface Detection) z Electronics: DAE3 Sn522; Calibrated: 9/11/2002 z Phantom: SAM 12; Type: TP-1217; Serial: QD000P40CA z Measurement SW: DASY4, V4.1 Build 47; Postprocessing SW: SEMCAD, V1.6 Build 115 _ (250 mW)/Area Scan (101x161x1): Measurement grid: dx=10mm, dy=10mm Reference Value = 55.5 V/m Power Drift = 0.009 dB Maximum value of SAR = 3.03 mW/g _ (250 mW)/Zoom Scan (7x7x7)/Cube 0: Measurement grid: dx=5mm, dy=5mm, dz=5mm Peak SAR (extrapolated) = 4.05 W/kg SAR(1 g) = 2.8 mW/g; SAR(10 g) = 1.79 mW/g Reference Value = 55.5 V/m Power Drift = 0.009 dB Maximum value of SAR = 3.02 mW/g 0 dB = 3.02mW/g ___________________________________________________________________________________________________ -ETS- DR. GENZ GMBH STORKOWER STRASSE 38c,D-15526 REICHENWALDE B. BERLIN TELEPHONE +49-33631-888 00 TELEFAX +49-33631-888 660 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ELECTRONIC TECHNOLOGY SYSTEMS DR. GENZ GMBH - ETS - STORKOWER STRASSE 38c, D-15526 REICHENWALDE B. BERLIN Tel: 033631 888 00 FAX: 033631 888 660 D2: 1800MHz SYSTEM VALIDATION DIPOLE C C C A A A L L L I I I B B B R R R A A A T T T I I I O O O N N N C C C E E E R R R T T T I I I F F F I I I C C C A A A T T T E E E 1800 MHz System Validation Dipole (Muscle) Type: D1800V2 Serial Number: 2d046 Place of Calibration: Reichenwalde Date of Calibration:September 05, 2003 Calibration Interval: 24 month ETS Dr. Genz GmbH hereby certifies, that this device has been calibrated on the date indicated above. The calibration was perf…

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RF Exposure Info

ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-S-1 Appendix C Appendix C. Pictures ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-S-1 Appendix C ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-S-1 Appendix C Valid 850 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-S-1 Appendix C Liquid depth 850 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-S-1 Appendix C Valid 900 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-S-1 Appendix C Liquid depth 900 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-S-1 Appendix C Valid 1800 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-S-1 Appendix C Liquid depth 1800 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-S-1 Appendix C Valid 1900 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-S-1 Appendix C Liquid depth 1900 ELECTRONIC TECHNOLOGY SYSTEMS DR.GENZ GMBH ETS Dr. Genz GmbH, Germany Registration number: G0M20512-0062-S-1 Appendix C

Test Report

Hermon Laboratories Ltd. P.O.Box 23, Binyamina 30500, Israel Tel. +972 4628 8001 Fax. +972 4628 8277 E-mail: [email protected] Page 1 of 153 Report ID: MOTRAD_FCC.16719_rev1.doc Date of Issue: November 2005 Electrical TEST REPORT ACCORDING TO: FCC parts 22, 24 and part 15 subpart B FOR: Motorola Communications Israel Ltd. QuadBand GSM module 850/1900 MHz Model:G24 FCC ID:IHDT56FV1 This report is in conformity with ISO/ IEC 17025. The A2LA logo endorsement applies only to the test methods and the standards that are listed in the scope of Hermon Laboratories accreditation. The test results relate only to the items tested. This test report shall not be reproduced in any form except in full with the written approval of Hermon Laboratories Ltd. Report ID: MOTRAD_FCC.16719_rev1.doc Date of Issue: November 2005 Page 2 of 153 Table of contents 1 Applicant information..................................................................................................................................................... 3 2 Equipment under test attributes .................................................................................................................................... 3 3 Manufacturer information .............................................................................................................................................. 3 4 Test details.................................................................................................................................................................... 3 5 Tests summary.............................................................................................................................................................. 4 6 EUT description............................................................................................................................................................. 5 6.1 General information....................................................................................................................................................... 5 6.2 Support and test equipment .......................................................................................................................................... 5 6.3 Operating frequencies ................................................................................................................................................... 5 6.4 Changes made in the EUT ............................................................................................................................................ 5 6.5 Transmitter characteristics ............................................................................................................................................ 6 7 Transmitter tests according to 47CFR part 22 requirements......................................................................................... 7 7.1 Peak output power ........................................................................................................................................................ 7 7.2 Occupied bandwidth test ............................................................................................................................................. 10 7.3 Spurious emissions at RF antenna connector test ..........................................................................................…

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Contact Information

Applicant

Dirk Koenig(Senior Manager Regulatory Affairs)
[email protected]+49-30-68905-0Fax: +49-30-68905-1921

Test Firm

Eurofins Product Service GmbHRobert Kschiwan-Kaspar
[email protected]49-33631-888-000Fax: 49-33631-888-660

Technical Specifications

#Rule PartsFrequency RangePower OutputEmissionTolerance
222H824.2 MHz - 848.8 MHz1.028 W283KGXW2.5 ppm
Confidentiality
Long Term
Grant Notes
Power output listed is ERP for Part 22 and EIRP for Part 24. SAR compliance for body-worn operations is restricted accessories supplied or designated for this product. Use of other accessories may not ensure compliance with FCC RF exposure guidelines. End-users must be informed of the body-worn operating requirements for satisfying RF exposure compliance. The highest reported SAR level is: Body-worn: 1.03 W/kg is for test position 1.5cm. This device contains 900 MHz GSM and 1800 DCS functions that are not operational in U.S. territories.

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