Medtronic MiniMed 7306 CareLINK USB User Manual
Medtronic MiniMed, Inc. CareLINK USB Users Manual
Users Manual
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| Document ID | 2526504 |
| Application ID | w9V0q43ZYbW8FQyh1qAblQ== |
| Document Description | Users Manual |
| Short Term Confidential | No |
| Permanent Confidential | No |
| Supercede | No |
| Document Type | User Manual |
| Display Format | Adobe Acrobat PDF - pdf |
| Filesize | 106.47kB (1330841 bits) |
| Date Submitted | 2015-02-06 00:00:00 |
| Date Available | 2015-02-09 00:00:00 |
| Creation Date | 2013-12-05 14:47:51 |
| Producing Software | Adobe PDF Library 10.0.1 |
| Document Lastmod | 2013-12-05 15:09:35 |
| Document Title | Users Manual |
| Document Creator | Adobe InDesign CS6 (Windows) |
CareLink™ USB User Guide Indications for use English The Medtronic CareLink™ USB (MMT-7306) is indicated for use by patients at home and clinicians in a medical office setting to facilitate communication between Medtronic diabetes therapy management devices (600-series) and a personal computer that uses Medtronic therapy management software for diabetes. Contraindications None known. Warnings Product may pose a choking hazard for young children. Getting Started IMPORTANT: If the CareLink USB drivers are not yet installed, or if you are not sure if the drivers are installed, do not connect the CareLink USB. See the instructions below for installing the CareLink USB drivers. Healthcare professionals: If you are a healthcare professional using CareLink™ Pro Therapy Management Software for Diabetes, the CareLink USB drivers will be installed as part of the CareLink Pro program installation. Patients: If you are a patient using CareLink™ Personal Therapy Management Software for Diabetes, you must follow these instructions BEFORE connecting the CareLink USB to your computer. Note: If you are not using Windows Vista, Windows 7, Windows 8 or Windows 8.1, continue directly with step 2. 1. Make sure that User Account Control is enabled. By default, User Account Control is already enabled, so it is likely that you do not have to enable it. a. Close Internet Explorer. (If you are using Windows 8 or 8.1, close Internet Explorer and do not use Internet Explorer from the start screen.) b. Navigate to Start > All Programs (or Programs). (If you are using Windows 8 or 8.1, from the Start screen, click on the Desktop tile.) c. Right-click on the Internet Explorer menu item. (If you are using Windows 8 or 8.1, right-click on the Internet Explorer icon from the task bar. Then right-click on Internet Explorer in the pull-up menu.) d. Select Run as Administrator. e. When the User Account Control window is displayed, click Allow or Yes. Note: If you are not logged in as an administrator on your computer, you may be asked to enter an administrator user’s password. 2. Navigate to the CareLink Personal website and register. • U.S. residents, use https://carelink.minimed.com • Non-U.S. residents, use https://carelink.minimed.eu Once registered, you will be able to sign in and upload your device data. 3. Click the Upload tab or Upload data from My Device link and follow the on-screen instructions. 4. If you need more assistance, click the Help link near the top of the screen. Connecting the CareLink USB to your computer Plug the CareLink USB into your computer when prompted by the CareLink software. It is recommended that the CareLink USB be plugged directly into a USB port on your computer, rather than into a peripheral device, such as a USB port on your monitor or keyboard. You can use a USB extension cable if you do not have easy access to the USB ports on your computer, but it is recommended that you use only a USB cable with a protected female end (see image). Troubleshooting • If you plug your CareLink USB into a USB port on your computer and it does not work, remove it and plug it into another USB port on your computer. If your CareLink USB does not work in any USB port on your computer, call the HelpLine for assistance or your local Medtronic representative. • Electrostatic discharge (ESD) may temporarily prevent the CareLink USB from functioning. If you touch the metal components of the CareLink USB or the uncovered end of a USB cable while it is connected to your computer, and your CareLink USB stops transmitting, remove it and plug it back in, being careful not to touch the metal parts. • If you are a healthcare professional, see the CareLink Pro User Guide for more information about supported devices, troubleshooting, or other instructions. • This device cannot be used to upload pumps other than the MiniMed 600-series pumps. Compliance information This device complies with the United States Federal Communications Commission (FCC) and international standards for electromagnetic compatibility. The CareLink USB (MMT-7306) conforms to the essential requirements of the Council Directive 1999/5/EC (R&TTE). The following information is provided in accordance with Federal Communications Commission (FCC) regulations. This device complies with Part 15 of the FCC Rules. 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 undesirable operation. This device does not interfere with any radio frequency signals transmitted from outside sources. These FCC standards are designed to provide reasonable protection against excessive radio frequency interference and prevent undesirable operation of the device from unwanted electromagnetic interference. IMPORTANT: Changes or modifications not expressly approved by Medtronic Minimed, Inc. could void the user’s authority to operate the equipment. RF interference from other wireless devices Common consumer electronic devices that transmit in the same frequency band used by the CareLink USB (MMT-7306) may prevent the CareLink USB from receiving the data sent by Medtronic diabetes therapy management devices. If significant RF interference is present, the CareLink USB and the device it is communicating with will switch to another channel and communications will continue. This equipment has been tested and found to comply with the limits for a Class B digital 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 installed 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 increasing the separation between the equipment and receiver. In the unlikely event that communications does not resume by switching to other channels, communication problems can typically be resolved by ensuring that the distance between transmitter and receiving device is less than 1.8 meters (6 feet), and by turning off or moving away from other RF transmitting devices. You can also reorient or relocate the CareLink USB and/ or the transmitting device to try to correct the interference. Note that RF interference will not cause any incorrect data to be processed and will not cause any harm to your CareLink USB. This device complies with Industry Canada licence-exempt RSS standard(s). Operation is subject to the following two conditions: (1) this device may not cause interference, and (2) this device must accept any interference, including interference that may cause undesired operation of the device. Le présent appareil est conforme aux CNR d’Industrie Canada applicables aux appareils 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. Wireless coexistence summary The CareLink USB (MMT-7306) was tested against the data listed in the two tables for wireless phones and wireless networks. The test results are described after the two tables. Wireless phones Telephones Frequency Recommended Separation Distance (meters) Recommended Separation Distance (inches) WCDMA 0.3 12 TDMA 0.3 12 0.3 12 0.254 10 GSM DECT 800 - 960 MHZ, 1700-2200 MHZ Wireless Networks Networks Frequency Recommended Separation Distance (meters) Recommended Separation Distance (inches) 802.11b/g/n 2.4 GHz 39 Bluetooth 2.4 GHz 0.1 3.93 ZigBee 2.4 GHz 0.1 3.93 Data integrity: Each interference event was evaluated for current and latent anomalies. The upload for each pump showed complete and uninterrupted functionality with no corrupted or missing data. Performance: The wireless functions operated safely and effectively in an intended use environment. Quality of service: • All of the wireless functions operated as intended. • All operations required of system-paired devices functioned as intended. • In an active RF environment, the system pairs identified and relocated to a clear channel within 3 minutes of uninterrupted download operation. Latency: The wireless function operated when commanded. There was no latency when establishing the wireless connection or transmitting data via the wireless connection in the adverse RF environment. Specifications Operating conditions Temperature: 5° C to 40° C. Humidity: 20% to 90%. Atmospheric pressure: 70.0 kPa to 106.0 kPa Storage conditions Temperature: -20° C to +55° C. Humidity: 5% to 95%, non-condensing. Atmospheric pressure: 49.5 kPa to 106.0 kPa Specifications Transmitter frequency 2.4 GHz Guidance and manufacturers declaration Table 1. Guidance and Manufacturers Declaration - Electromagnetic Emissions This CareLink USB (MMT-7306) is intended for use in the electromagnetic environment specified below. The customer or the user of the CareLink USB should make sure that it is used in such an environment. Emissions Test Compliance Electromagnetic Environment - Guidance The CareLink USB uses RF energy only for its internal function. Therefore, RF emissions CISPR 11 Group 1 its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment. RF emissions CISPR 11 Class B Harmonic emissions IEC 61000-3-2 Not applicable Voltage fluctuations/ flicker emissions IEC 61000-3-3 Not applicable The device is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage network that supplies buildings used for domestic purposes. Table 2. Guidance and Manufacturers Declaration - Electromagnetic Immunity This CareLink USB (MMT-7306) is intended for use in the electromagnetic environment specified below. The customer or the user of the CareLink USB should make sure that it is used in such an environment. IEC 60601 Test Compliance Immunity Test Electromagnetic Environment - Guidance Level Level Electrostatic ±4 kV contact ±4 kV contact The CareLink USB should not be affected by electrostatic discharge that discharge (ESD) might occur under normal conditions of use. IEC 61000-4-2 ±8 kV air ±8 kV air Table 2, continued next page Table 2. Guidance and Manufacturers Declaration - Electromagnetic Immunity This CareLink USB (MMT-7306) is intended for use in the electromagnetic environment specified below. The customer or the user of the CareLink USB should make sure that it is used in such an environment. IEC 60601 Test Compliance Immunity Test Electromagnetic Environment - Guidance Level Level Electrical fast transient/burst IEC 61000-4-4 Surge IEC 61000-4-5 Voltage dips, short interruptions and voltage variations on power supply lines IEC 61000-4-11 Power frequency (50/60 Hz) magnetic field IEC 61000-4-8 ±2 kV for power Not applicable supply lines ±1 kV for ±1 kV for input/ input/output output lines lines ±1 kV line(s) to ±1 kV line(s) to line(s) line(s) ±2 kV line(s) to ±2 kV line(s) to For use in a typical domestic, commercial, or hospital environment. earth earth 0% 0.5 cycles 0% 1 cycle 70% 25 cycles 0% 250 cycles 0% 0.5 cycles 0% 1 cycle 70% 25 cycles 0% 250 cycles 3 A/m 3 A/m Table 2, continued next page Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment. Table 2. Guidance and Manufacturers Declaration - Electromagnetic Immunity This CareLink USB (MMT-7306) is intended for use in the electromagnetic environment specified below. The customer or the user of the CareLink USB should make sure that it is used in such an environment. IEC 60601 Test Compliance Immunity Test Electromagnetic Environment - Guidance Level Level Conducted RF IEC 61000-4-6 3V rm 150kHz to 80 MHz 3V rms 150 kHz to 80 MHz Radiated RF IEC 61000-4-3 3V/m 80 MHz to 6 GHz 10V/m 80 MHz to 6 GHz Portable and mobile RF communications equipment should be used no closer to any part of the CareLink USB than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance d = 1.2 √P 80 MHz-800 MHz d = 2.3 √P 800 MHz-6 GHz Where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey,a should be less than the compliance level in each frequency range. b Interference may occur in the vicinity of equipment marked with the following symbol: NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies. NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption, and reflection from structures, objects and people. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcasts and TV broadcast cannot be predicted theoretically with accuracy. To access the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the CareLink USB is used exceeds the applicable RF compliance level above, the CareLink USB should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the CareLink USB or the transmitting device from which it is receiving signals. Over the frequency range 150 KHz to 80 MHz, field strengths should be less than 3 V/m. Table 3. Recommended separation distances between portable and mobile RF communications equipment and the CareLink USB This section provides information on the recommended separation distance between portable and mobile RF communications equipment and the CareLink USB. The CareLink USB is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the CareLink USB users can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the CareLink USB as recommended below, according to the maximum output power of the communications equipment. Separation distance according to the frequency of transmitter (m) Rated maximum output power of transmitter (W) 80 MHz to 800 MHz 800 MHz to 6 GHz d = 1.2 √P d = 2.3 √P 0.01 0.12 0.23 0.1 0.38 0.74 1.2 2.3 10 3.8 7.4 100 12 23 For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where p is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption, and reflection from structures, objects and people. Icon Table Symbol 10 Meaning Symbol Meaning Caution: Consult accompanying documents Manufacturer Consult instructions for use Date of manufacture Icon Table Symbol Meaning Meaning Device serial number Signifies compliance with Australian EMC, EME and Radio communications requirement Catalogue number Radio communication Humidity limitation Authorized representative in the European Community Storage temperature range (1x) Symbol IC Signifies compliance with Industry Canada EMC and Radio communications requirements One per container/package Complies with Japan Radio Law Notice 88 Manufacturing site This symbol means that the device fully complies with MDD 93/42/EEC and R&TTE Directive 1999/5/ EC. ©2013, Medtronic MiniMed, Inc. All rights reserved. CareLink™ is a trademark of Medtronic MiniMed, Inc. 11 Contacts: Africa: Medtronic Africa (Pty) Ltd. Tel: +27 (0) 11 677 4800 Australia: Medtronic Australasia Pty. Ltd. Tel: 1800 777 808 (cust. help) Tel: 1800 668 670 (orders) Bulgaria: Interagro-90 Ltd Tel: +359 888 636 033 Eire: Accu-Science LTD. Tel: +353 45 433000 Canada: Medtronic of Canada Ltd. Tel: 1-800-284-4416 España: Medtronic Ibérica S.A. Tel: +34 91 625 05 42 24 horas: +34 901 120 335 Azerbaijan: Albatros Health Care Tel: +994 12 498 9537 China: Medtronic (Shanghai) Ltd. 24 Hour HelpLine (Cell): +86 400-820-1981 24 Hour HelpLine (Land): +86 800-820-1981 Bangladesh: Sonargaon Healthcare Pvt Ltd. Mobile: (+91)-9903995417 or (+880)-1714217131 Croatia: Oktal Pharma Tel: +385 1 659 57 77 Fax: +385 1 659 57 01 Belarus: Badgin Ltd Tel: +375 (172) 665128 Croatia: Medtronic B.V. Tel: +385 1 488 11 20 Fax: + 385 1 484 40 60 België/Belgique: N.V. Medtronic Belgium S.A. Tel: 0800-90805 Bosnia and Herzegovina: Intermedical Tel: +387 33 202 183 Fax: +387 33 202 183 Brasil: Medtronic Comercial Ltda. Tel: +(11) 3707-3707 12 Danmark: Medtronic Danmark A/S Tel: +45 32 48 18 00 Deutschland: Medtronic GmbH Geschäftsbereich Diabetes Telefon: +49 2159 8149-370 Telefax: +49 2159 8149-110 24-Stdn-Hotline: 0800 6464633 Europe: Medtronic Europe S.A. Europe, Middle East and Africa HQ Tel: +41 (0) 21-802-7000 France: Medtronic France S.A.S. Tel: +33 (0) 1 55 38 17 00 Hellas: Medtronic Hellas S.A. Tel: +30 210677-9099 Hong Kong: Medtronic International Ltd. Tel: +852 2919-1300 To order supplies: +852 2919-1322 24-hour helpline: +852-2919-6441 India: India Medtronic Pvt. Ltd Tel: (+91)-80-22112245 / 32972359 Mobile: (+91)-9611633007 Indonesia: Medtronic International Ltd. Tel: +65 6436 5090 or +65 6436 5000 Macedonia: Kemofarm Tel: +389 2 260 36 03 Fax: +389 2 260 36 49 Philippines: Medtronic International Ltd. Tel: +65 6436 5090 or +65 6436 5000 Israel: Agentek Tel: +972 3649 3111 Magyarország: Medtronic Hungária Kft. Tel: +36 1 889 0688 Italia: Medtronic Italia S.p.A. Tel: +39 02 24137 261 Servizio assistenza tecnica: N° verde 24h: 800 20 90 20 Malaysia: Medtronic International Ltd. Tel: +603 7946 9000 POCCИЯ: Medtronic B.V. Tel: +7 495 580 73 77 24h: 8-800-200-76-36 Japan: Medtronic Japan Co. Ltd. Tel: +81-3-6430-2019 24 Hr. Support Line: 0120-56-32-56 Kazakhstan: Medtronic Kazakhstan B.V. Tel: +77273110580 Latin America: Medtronic, Inc. Tel: 1(305) 500-9328 Fax: 1(786) 709-4244 Latvija: Ravemma Ltd. Tel: +371 7273780 Middle East and North Africa: Regional Office Tel: +961-1-370 670 Montenegro: Glosarij Tel: +382 20 642 495 Fax: +382 20 642 540 Nederland, Luxembourg: Medtronic B.V. Tel: +31 (0) 45-566-8291 Gratis: 0800-3422338 New Zealand: Medica Pacifica Phone: 64 9 414 0318 Free Phone: 0800 106 100 Norge: Medtronic Norge A/S Tel: +47 67 10 32 00 Polska: Medtronic Poland Sp. Z.o.o. Tel: +48 22 465 6934 Portugal: Medtronic Portugal Lda Tel: +351 21 7245100 Fax: +351 21 7245199 Puerto Rico: Medtronic Puerto Rico Tel: 787-753-5270 Republic of Korea: Medtronic Korea, Co., Ltd. Tel: +82.2.3404.3600 Romania: Trustmed SRL Tel: +40 (0) 21 220 6477 Schweiz: Medtronic (Schweiz) AG Tel: + 41 (0) 31 868 0160 24-Stunden-Hotline: 0800 633333 13 Serbia: Epsilon Tel: +381 11 311 5554 Fax: +381 11 311 5554 Taiwan: Medtronic-Taiwan Ltd. Tel: +886.2.2183.6068 Toll Free: +886.0800.005.285 Singapore: Medtronic International Ltd. Tel: +65 6436 5090 or +65 6436 5000 Thailand: Medtronic (Thailand) Ltd. Tel: +662 232 7400 Slovenija: Zaloker & Zaloker d.o.o. Tel.: +386 1 542 51 11 24-h pomoč: +386 51 316 560 Slovenská republika: Medtronic Slovakia o.z. Tel: +421 26820 6986 Sri Lanka: Swiss Biogenics Ltd. Mobile: (+91)-9003077499 or (+94)-777256760 Suomi: Medtronic Finland Oy Tel: +358 20 7281 200 Help line: +358 400 100 313 Sverige: Medtronic AB Tel: +46 8 568 585 10 14 Turkiye: Medtronic Medikal Teknoloji Ticaret Ltd. Sirketi. Tel: +90 216 4694330 Ukraine: Med EK Service Ltd. Tel: +380445457705 USA: Medtronic Diabetes Global Headquarters Tel: +1-800-646-4633 24 Hour HelpLine: +1-800-826-2099 To order supplies: +1-800-843-6687 United Kingdom: Medtronic Ltd. Tel: +44 1923-205167 Österreich: Medtronic Österreich GmbH Tel: +43 (0) 1 240 44-0 24 – Stunden – Hotline: 0820 820 190 Česká republika: Medtronic Czechia s.r.o. Tel: +420 233 059 401 Non-stop help line: +420 233 059 059 15 REF MMT-7306 6025822-21A1P_1
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