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QBI-1010Wireless Modem

Cardionet
Wireless Modem - FCC ID QBI-1010 - Cardionet
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Application Details

Equipment Class
DTS - Digital Transmission System
Date of Grant
Mar 28, 2007
Application Purpose
Original Equipment
Date of Application
Mar 28, 2007
Equipment Note
Wireless Modem
Frequency Range
902.96000000 - 926.24000000
Company
Cardionet
Country
United States

Documents & Files

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Users Manual

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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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Operational Description

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Parts List/Tune Up Info

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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

Patient Education Guide CardioNet Ambulatory ECG System and Arrhythmia Detector Manufactured by CardioNet Inc. 1010 Second Ave., Suite 700 San Diego, CA 92101 Copyright 2006 All rights reserved Document number 101010 Revision B October 2006 M O B I L E C A R D I A C O U TP AT I E N T T E L E M E T RY 2 1 3 I N T R O D U C T I O N . . . . . . . . . . . . . . . . . . . . . . . .1 How the CardioNet Service Works. . . . . . . . . . . . . . . . . . .2 Your CardioNet Monitoring Supplies . . . . . . . . . . . . . . . . .4 Your Rights as a Patient. . . . . . . . . . . . . . . . . . . . . . . . . .6 Your Responsibilities as a Patient . . . . . . . . . . . . . . . . . . .6 Who to Call with Questions . . . .. . . . . . . . . . . . . . . . . . .6 In the Case of an Emergency. . . . . . . . . . . . . . . . . . . . . .7 What to Do When your Monitoring is Over. . . . . . . . . . . . .8 G E T T I N G S TA RT E D . . . . . . . . . . . . . . . . . . . . .9 Connecting from Home . . . . . . .. . . . . . . . . . . . . . . . . . 10 How to Install the CardioNet Base . . . . . . . . . . . . . . . . .11 About the CardioNet Base . . . . .. . . . . . . . . . . . . . . . . . 14 How to Activate the CardioNet Sensor . . . . . . . . . . . . . . .15 Tips for Wearing the CardioNet Sensor . . . . . . . . . . . . . .18 How to Activate the CardioNet Monitor . . . . . . . . . . . . . .19 U S I N G T H E M o n i t o r . . . . . . . . . . . . . . . . . . . .2 5 How to Turn your Monitor On and Off . . . . . . . . . . . . . . .26 How to Record an Event . . . . . .. . . . . . . . . . . . . . . . . . 28 How to Change Monitor Options . . . . . . . . . . . . . . . . . . . 30 How to Check Battery Power . . .. . . . . . . . . . . . . . . . . . 34 How to Check Cell Phone Coverage . . . . . . . . . . . . . . . .35 Receiving Messages from CardioNet . . . . . . . . . . . . . . . .36 How to Read a Text Message. . . . . . . . . . . . . . . . . . . . . 37 ii Table of Contents T A B L E O F C O N T E N T S 4 5 6 S E N S O R C A R E . . . . . . . . . . . . . . . . . . . . . . . .3 9 Tips for Changing Electrode Pads. . . . . . . . . . . . . . . . . . 40 How to Change Electrodes and Attach Sensor . . . . . . . . .41 Remove Before Showering or Bathing . . . . . . . . . . . . . . .44 How to Change the Sensor AA Battery . . . . . . . . . . . . . .45 T R O U B L E S H O O T I N G . . . . . . . . . . . . . . . . . . .4 7 Responding to Monitor Alerts and Alarms . . . . . . . . . . . .48 Troubleshooting Device Problems. . . . . . . . . . . . . . . . . . 51 Precautions . . . . . .. . . . . . . . . . . . . . . . . . . . . . . . . . . 53 Cautions . . . . . . . .. . . . . . . . . . . . . . . . . . . . . . . . . . . 54 Warnings . . . . . . . .. . . . . . . . . . . . . . . . . . . . . . . . . . . 55 S P E C I F I C AT I O N S , C O M P L I A N C E & S Y M B O L S 5 7 Specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58 Equipment Symbols. . . . . . . . . . . . . . . . . . . . . . . . . . . . 60 In Home Requirements . . . . . . .. . . . . . . . . . . . . . . . . . 60 FCC Compliance . . .. . . . . . . . . . . . . . . . . . . . . . . . . . . 62 Table of Contents iii 1 β€’ How the CardioNet Service Works β€’ Your CardioNet Monitoring Supplies β€’ Your Rights as a Patient β€’ Your Responsibilities as a Patient β€’ Who to Call with Questions β€’ In the Case of an Emergency β€’ What to Do When your Monitoring is Over I N T R O D U C T I O N In this Chapter:  Introduction When you’re using the CardioNet service, you’ll wear a small, lightweight sensor on your chest. The sensor detects and analyses each heartbeat and sends data to the p o r t a b l e C a r d i o N e t monitor. The CardioNet monitor can be tucked away in a pocket or purse. When the sensor detects an event, or when you report an event using the touch screen on the monitor, it transmits the data to the CardioNet Monitoring Center. 12 Monitor transmits eventsSensor detects and analyses heartbeats How the CardioNet Service Works 1 . I N T R O D U C T I O N Introduction  3 The CardioNet Monitoring Center operates 24 hours a day, 7 days a week. At the Center, specially trained cardiac technicians analyze your heart rhythms and report results to your physician. Your physician reviews the report, discusses results with you and prescribes or adjusts treatment as needed. 4 CardioNet reports to your physician Your physician reviews your results How the CardioNet Service Works 1 . I N T R O D U C T I O N  Introduction PictureItem and Description CARDIONET SHIPPING KIT The CardioNet shipping kit contains all the items you will need during your monitoring service. You can also reference the inside lid of the kit for information on where each item is located in the kit. CARDIONET SENSOR The sensor can be worn around the neck or on a belt. It detects each heartbeat and sends data to the CardioNet monitor. To communicate with the monitor, the sensor must remain close to the monitor. Walls and other obstructions can interfere with the communications between the sensor and the monitor. If you go out of communications range, the sensor and monitor will beep to alert you. CARDIONET Monitor The monitor constantly analyzes data from the sensor and sends events to the CardioNet Monitoring Center. The monitor uses wireless communication when not in the base and uses the regular phone system when the monitor is placed in the base. You will not be charged by the telephone company for calls made by your monitor. CARDIONET BASE The base recharges the CardioNet monitor and allows the monitor to communicate with the Monitoring Center using your home phone system. The bases are connected to your phone line and plugged into electrical outlets in your bedroom and another room in your home. The CardioNet Kit The CardioNet Kit contains the supplies you will need while you are on the CardioNet Monitoring Service. If any items are missing or broken, or if you have any questions about how to use them, please call CardioNet …

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ID Label/Location Info

CARDIONET BASE PROPERTY OF CARDIONET, INC. SAN DIEGO, CA 92101 IF FOUND PLEASE CALL: (866) 426-4404 100-0024-01 FCC ID: QBI-1010 (ISM RF) THIS DEVICE COMPLIES WITH PART 15 AND 68 OF THE FCC RULES. OPERATION IS SUBJECT TO THE FOLLOWING TWO CONDITIONS: (1) THIS DEVICE MAY NOT CAUSE HARMFUL INTERFER- ENCE AND, (2) THIS DEVICE MUST ACCEPT INTERFERENCE RECEIVED INCLUDING INTERFERENCE THAT MAY CAUSE UNDESIRED OPERATION. SPECIFICATIONS NOTES Please check design, copy, critical placements and specifications carefully. Take note of our "Warranty and Limited Liability" statement below. Check appropriate box below, sign and return so we may proceed with your order. Your signature: Your account manager is: Print as is Print with corrections marked Submit corrected proof Part Number: P.O. Number: Qty Ordered: GM Number: Finished Size: Approval of this proof is required by to maintain your scheduled ship date. Save time in contacting GM Nameplate, Inc. Phone: 408-435-1666 Fax: 408-435-8121 Customer alterations of original design are not included in quotation. Changes made at this point in production may result in additional charges. Please Note: Die line per supplied file black sequential 128 barcode and serial numbers starting at B80001 to be added in white box 220-0053-01 Rev 1 5029 4000 055619 2.560" x 3.710" Pam Hane Please notify your account manager immediately if there are any changes. Customer:Cardionet3-16-07 3rd Proof Attn: Phil Lamb Please Note: The colors shown are not for color matching purposes. They are for reference only. = Cardionet Gray = PMS 3125C = white graphics = die line Warranty and Limited Liability: GM Nameplate makes no warranty as to its products or service (whether express, implied or statutory) including but not limited to, the warranty of merchantability, the warranty of fitness for a particular purpose, and any implied warranty arising out of course of dealing, customer use or trade, except that GM Nameplate warrants its products will be free from defects in materials and workmanship in normal use and service. If a product is proved to be defective, then the exclusive remedy, and GM Nameplate's sole obligation, shall be GM Nameplate's option to replace that quantity of product which is proved to be defective or refund the purchase price for that portion of the product to be defective. Limitation of Liability: GM Nameplate shall not be liable for direct, indirect, special, accidental or consequential damages based upon breach of warranty, breach of contract, negligence, strict liability or any other legal theory. The foregoing Warranty and Limited Remedy and Limitation of Liability may be changed only by written agreement signed by an authorized officer of GM Nameplate. 3-19-07 GM Nameplate Art Proof gray background blue and white graphics die line will not print WARNING: PROTECT FROM WATER AND OTHER LIQUIDS. 15 VOLTS DC, 1.2 AMPS. USE ONLY WITH CARDIONET APPROVED POWER PLUG.

Operational Description

Base Operational Description The C-3 Base is a small table top device that is used to communicate with the C-3 Monitor using the 900 MHz radios in both these devices. The C-3 Base also acts as a charger. An AC to DC converter is plugged into the wall to provide 15V, 1.0A power to the Base. This power is passed on to the Monitor to charge its batteries when plugged into the Base. The Base communicates with the Monitoring Center through the Plain Old Telephone System (POTS). The Base has a FCC Part 68 approved standard 57.6 Kbaud Modem and this provides standard telephone line communications. The Base is designed around a low power 16 bit TI MSP-430 processor, power supply, a 900 MHz radio module and a small Multitech modem module. The Base has a helical spring antenna to communicate with the Monitor. The antenna ground plane is isolated from mains ground by an AC adapter.

RF Exposure Info

Prediction of MPE limit at a given distance Equation from page 18 of OET Bulletin 65, Edition 97-01 where:S = power density P = power input to the antenna G = power gain of the antenna in the direction of interest relative to an isotropic radiator R = distance to the center of radiation of the antenna Maximum peak output power at antenna input terminal:15.62(dBm) Maximum peak output power at antenna input terminal:36.47539469(mW) Antenna gain(typical):0(dBi) Maximum antenna gain:1(numeric) Time Averaging:100(%) Prediction distance:20(cm) Prediction frequency:926.24(MHz) MPE limit for uncontrolled exposure at prediction frequency:0.6(mW/cm^2) Power density at prediction frequency:0.0072565492082(mW/cm^2) Margin of compliance:-19.2(dB) 2 4R PG S Ο€ =

Test Report

Nemko USA, Inc. 11696 Sorrento Valley Rd., Suite F San Diego, CA 92121-1024 Phone (858) 755-5525 Fax (858) 452-1810 FCC Part 15 Subpart C, 15.247 : 27/03/2007 Test Report: 2007 012630 C3 FCC Project number: 2630 Applicant: Cardionet 1010 Second Ave. Suite 700 San Diego, CA 92101 Equipment Under Test (EUT): Wireless Modem Model: C3 Base FCC ID: FCC ID: QBI-1010 In Accordance With: FCC Part 15 Subpart C, 15.247 Tested By: Nemko USA Inc. 11696 Sorrento Valley Road, Suite F San Diego, CA 92121 Authorized By: Michael T. Krumweide, EMC Supervisor Date: FEBRUARY 2, 2007 Total Number of Pages: 39 Nemko USA, Inc. 11696 Sorrento Valley Road, Suite F, San Diego, CA 92121 Phone (858) 755-5525 Fax (858) 452-1810 Report Number: 2007 012630 C3 FCC FCC ID: FCC ID: QBI-1010 Specification: FCC Part 15 Subpart C, 15.247 Page 2 of 39 2.1. Section 1. Summary of Test Results General All measurements are traceable to national standards These tests were conducted on a sample of the equipment for the purpose of demonstrating compliance with Part 15; Subpart C. Radiated tests were conducted is accordance with ANSI C63.4-2003. Radiated emissions are made on an open area test site. A description of the test facility is on file with the FCC. The assessment summary is as follows: Apparatus Assessed: Wireless Modem Model C3 Base Specification: FCC Part 15 Subpart C, 15.247 Date Received in Laboratory: January 29, 2007 Compliance Status: Complies Exclusions: None Non-compliances: None Report Release History: REVISION DATE COMMENTS - February 2, 2007 Prepared By: Ferdinand S. Custodio - February 2, 2007 Initial Release: Mike T. Krumweide Note that the results contained in this report relate only to the items tested and were obtained in the period between the date of initial receipt of samples and the date of issue of the report. This test report has been completed in accordance with the requirements of ISO/IEC 17025. Nemko USA, Inc. 11696 Sorrento Valley Road, Suite F, San Diego, CA 92121 Phone (858) 755-5525 Fax (858) 452-1810 Report Number: 2007 012630 C3 FCC FCC ID: FCC ID: QBI-1010 Specification: FCC Part 15 Subpart C, 15.247 Page 3 of 39 Nemko USA Inc. authorizes the applicant to reproduce this report provided it is reproduced in its entirety and for use by the company’s employees only. Any use which a third party makes of this report, or any reliance on or decisions to be made based on it, are the responsibility of such third parties. Nemko USA Inc. accepts no responsibility for damages, if any, suffered by any third party as a result of decisions made or actions based on this report. TESTED BY: ___________________________________ Date: February 2, 2007 Ferdinand S. Custodio, EMC Test Engineer Nemko USA, Inc. 11696 Sorrento Valley Road, Suite F, San Diego, CA 92121 Phone (858) 755-5525 Fax (858) 452-1810 Report Number: 2007 012630 C3 FCC FCC ID: FCC ID: QBI-1010 Specification: FCC Part 15 Subpart C, 15.247 Page 4 of 39 TABLE OF CONTENTS 2.1. Section 1. Summary of Test Results.......................................................................2 Section 2: Equipment Under Test..........................................................................................6 2.1 Product Identification...................................................................................................6 2.2 Samples Submitted for Assessment.........................................................................6 2.4 Theory of Operation.....................................................................................................7 2.5 Technical Specifications of the EUT.........................................................................7 2.6 General Test Configuration.........................................................................................8 Section 3: Test Conditions......................................................................................................9 3.1 Specifications................................................................................................................9 3.2 Deviations From Laboratory Test Procedures.........................................................9 3.3 Test Environment.........................................................................................................9 3.4 Test Equipment...........................................................................................................10 Section 4: Observations.........................................................................................................11 4.1 Modifications Performed During Assessment........................................................11 4.2 Record Of Technical Judgements...........................................................................11 4.3 EUT Parameters Affecting Compliance..................................................................11 4.4 Test Deleted................................................................................................................11 4.5 Additional Observations............................................................................................11 Section 5: Results Summary.................................................................................................12 5.1 FCC Part 15 Subpart C: Test Results.....................................................................12 Appendix A: Test Results......................................................................................................13 Clause 15.209(a) Radiated Emissions within Restricted Bands.........................................13 Clause 15.247(a)(2) Minimum 6dB RF Bandwidth...............................................................16 Bandedge Measurements.........................................................................................................20 Clause 15.247(b)(3) Maximum peak output power of systems using digital modulation in the 902-928 MHz, 2400-2483.5 MHz, and 5725-5850 MHz bands......................…

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Contact Information

Applicant

Kent Sayler(Quality/Regulatory VP)
[email protected]619 243 7560Fax: 619 243 7700

Technical Contact

Nemko USA, Inc.Harry Ward
[email protected](972) 436-9600

802 N. Kealy Ave Β· Lewisville, Texas Β· United States

Non-Technical Contact

Nemko USA, Inc.Christine Taylor
[email protected](972) 436-9600

Test Firm

Nemko USA, Inc.Tom Tidwell
[email protected]9724369600Fax: 9724362667

Technical Specifications

#Rule PartsFrequency RangePower Output
115C902.96 MHz - 926.24 MHz36.40 mW
Confidentiality
Long Term
Grant Notes
Power listed is conducted. The antenna used for this transmitter must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter. End-users and installers must be provided with antenna installation and transmitter operating conditions for satisfying RF exposure compliance.

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