T3W-MUMS-002Multi-users, multi-sensors

Multi User Multi Sensors Model MUMS-002 Operator’s Manual 6700, avenue Choquette bur. 200 St-Hyacinthe (Québec) J2S 8L1 Tél: 1-866-550-1414 Fax: (450) 250-1416 www.telemedic.ca Copyright © 2010 TéléMédic Inc. All rights reserved. This equipment is protected by the Canadian copyright laws. It cannot be reproduced, distributed or modified in any ways by other entities than TéléMédic, except under written consent by TéléMédic. All the requisite efforts have been done to ensure that the information contained in this document was complete and precise at the moment of printing. However, the information can be modified without notice. Declaration of conformity This device is registered as CSA International certified. To see the certificates of official declaration, consult the online documentation on TéléMédic’s website: http : //www.telemedic.ca This device complies with Industry Canada’s low power radio devices norms RSS-210. Certification number: 6418A-MUMS002 This device complies with the FCC (Federal Communications Commission) intentional radio frequencies transmission. Identification number: FCC ID : T3W -MUMS-002 Trademark Vie-Gie Med is registered trademarks. Other brands and products names mentioned in this document are properties of the respective holders. Ordering information You can order updates of this document directly on TéléMédic's website: http://www.telemedic.ca . Comments TéléMédic appreciates your comments relating to this manual. Please send your comments directly to [email protected]. Support For all technical questions or defectiveness, please contact TéléMédic’s user support service at 1-866-550-1414 or at [email protected] Meaning of symbols used in this manual: Warning: Failure to these instructions may lead to unexpected operation or defects of the system. Important: Important element to consider in the use of this device. Meaning of device symbols: Warning: Consult accompanying documents. This manual and the associated sections on TéléMédic’s website (see manual for references) should be consulted before using this device. This equipment complies with general requirements for safety of medical electrical equipment CAN/CSA C22.2 No.601.1 and CAN/CSA C22.2 No.60601-1-1, UL 2601-1. This equipment also complies with electromagnetic compatibility requirements for medical electrical equipment CAN/CSA C22.2 No 60601-1-2 This device complies with FCC (Federal Communications Commission) rules part 15 (Radio frequency devices) for the United States. This equipment includes radio frequency transmitter which generate non-ionizing radiation. Table of contain The Multi User Multi Sensors, MUMS ............................................................................................................. 4 Indications for use............................................................................................................................................ 4 Main components ............................................................................................................................................ 4 Installation....................................................................................................................................................... 6 Turning on the unit....................................................................................................................................... 6 MUMS indicators ............................................................................................................................................ 6 Language selection .......................................................................................................................................... 7 Acquiring vital signs session ............................................................................................................................ 8 Emergency stop ............................................................................................................................................... 8 Server data transmission .................................................................................................................................. 8 Battery recharge (available only on model MUMS-002)................................................................................... 8 Precautionary measures.................................................................................................................................... 8 Functional preventive check-ups ...................................................................................................................... 9 Maintenance .................................................................................................................................................... 9 Optimal operating performance ........................................................................................................................ 9 Warranty ........................................................................................................................................................... 9 Technical support ............................................................................................................................................ 10 Conformity....................................................................................................................................................... 10 Technical specifications ................................................................................................................................... 11 Pictures list Picture 1: Components of MUMS ........................................................................................................................ 4 Picture 2: Accessories port of MUMS .................................................................................................................. 5 Table list Table 1 List of supported optional medical equipment…

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Nemko Canada lnc 303 River Road Ottawa, Ontario, Canada K1V 1H2 Attn: Director of Certification Authoritv to Act as Aqent On our behalf, I appoint Nemko Canada lnc., 303 River Road, Ottawa, Ont. to act as our agent in the preparation of this application for equipment certification. I certify that submitted documents properly describe the device or system for which equipment certification is sought. I also certify that each unit manufactured, imported or marketed, as defined in the Federal Communications Commission's regulations will have affixed to it a label identical to that submitted for approvalwith this application. For instances where our authorized agent signs the application for certification on our behalf, I acknowledge that all responsibility for complying with the terms and conditions for certification, as specified by Nemko Canada Inc, still resides with TéléMédic Inc., 6700 Choquette, bur.200, Saint-Hyacinthe, Qc.. Dated 17 this Day of May 20 10 Agency "nryWt eyiration date: ,l',t {'/ By: /i l---'\ 12 Months André Junior Richard Signature Title: Electronic Department Superuisor On behalf of : TéléMédic Inc. Telephone: 450-250-1414 Printed

Equipment Autorisation Division Federal Communications Commission 7435 Oakland Mills Road Columbia, MD 21046 FCC lD: T3W-MUMS-002 Product Name: MUMS-002 Request for Confidentialitv Pursuant to Sections 0.457 and 0.459 of the commissions rules, we hereby request that the following documents be held confidential: o Block diagram . Schematics . OperationalDescription . Parts Lists These materials contain trade secrets and proprietary information and are not customarily released to the public. The public disclosure of this information might be harmful to the company and provide unjustified benefits to our competitors. Dated this 28Day of May20 10 André Junior RichardBy: Printed Title: Electronic Depaftment Supervisor On behalf of :TéléMédic Inc. Telephone: 450-250-1411 Signature

S01-10-115.doc Page(lde3) ÆppÆcuvr Nom du produit / assemblage / sous assemblage : Assemblage 20-021 L'étiquette suivante sert à identifier le produit20-021. Cette étiquette sera placée sous le boîtier de I'unité. L'étiquette doit êtrc de type autocollant Dimensions : (1 .25" X 2,7 5" ) maximum Étiquette proposée**: Compagnie: BRADY Matériel: Polyester # catalog ue : T HT -7 423-3 Utiliser avec ruban 6000 **L'étiquette utilisée peut être différente de celle proposée mais doit similaire et approuvé CSA. Le choix de l'étiquette devra également être approuvé par Télémédic avant d'être utilisé. Modification avant certification CSA Les renseignements suivants doivent apparaître sur l'étiquette: Le nom de l'instrument (Modèle) et sa révision, le nom et I'adresse web du fabricant, numéro de contrôle (S/N), l.D. numéro unique des appareils (M93 et l9X), un code bar (CODE 128) pour le lD du lgx E un code bar (CODE 128) pour le lD de la M93 bien identifié a chaque appareil. Les codes à barre doivent avoir une résolution d'au moins 7 mil. Symboles d'avertissement et de radiation RF non ionisante Numéro d'industrie Canada lC : 64184-MUMS002 Numéro d'identification FCC FCC lD : T3W-MUMS-002 Logo "CSA,, et FCC Déclaration de conformité (DOC) Logo < Body Field > Logo < alarme éteinte/pas d'alarmes > représenté par un triangle avec une barre. Description du numéro de contrôle (numéro de série) Ex : 50050001 (LLAAUUUU) . LOT : (LL) deux décimales - ldentification du lot de fabrication. Le numéro se réinitialise au début de chaque année. o Année de I'ordonnancement : (AA) deux décimales o Unité: (UUUU) quatre décimales - Numéro d'identification de I'unité. Le numéro est remis à un (1) pour chaque nouveau LOT. Date: 21103106 Fichier: Q01-038 Rév: B $"**,- S01-10-115.doc t Page(2de3) .APPRSF'1 '"* Description du numéro d'identification (lD) Ex:1AFD75E o lD (XXXXXXX) : Contient le numéro de série utilisant 7 caractères alphanumériques: 0-9, A à Z IVIUM$-Û02 REV. 1 Telémédic lnt. r*nnnru.telemedic.ca $N: 17050007 ID M93: ID I9X: Fabriqué au / Made in Canada TTe dnics mm$ieeruidr Pâft 15 of$æ FCC ruhs. Wrdion is er$itctb {u fulltn*ting tm condtiæs: { 1) Th{e dwice mfiy rKû canes harmfr^{ lrûerbrcrue, and { 4 ûrin dev{ce mr.rd accçt any irilerfererue receiræd, irdudlng inbferenc* thd m4r cau*e un&rlnad ryerdi*r. FCC lD: T3W-MUMS-0û2 lC: ô4184-MUM$002 N $4**** S01-10-115.doc Page(3de3) ÆppR#{JyE' Apposer un échantillon de l'étiquette ci-dessous. Note : l'étiquette peut varier selon le lot de fabrication. Le positionnement de l'étiquette doit être comme suit : '%. #r{rR *-t bTrqueïTe ici Date:21103106 Fichier: QOl-038 Rév: B

www.nemko.com Report Reference ID: 146144-1TRFWL Test specification: Title 47 - Telecommunication Chapter I - Federal Communications Commission Subchapter A - General Part 15 - Radio Frequency Devices Subpart C - Intentional Radiators − §15.249 - Operation in the 902–928 MHz, 2400–2483.5 MHz, 5725–5875 MHz and 24.0–24.25 GHz Applicant: TeleMedic Inc. 6700 Choquette, bur. 200 St-Hyacinthe, QC J2S 8L1 Canada Apparatus: Telemedic MUMS-002 FCC ID: T3W-MUMS-002 Model: MUMS-002 Testing laboratory: Nemko Canada Inc. 303 River Road Ottawa, ON, Canada K1V 1H2 Telephone: (613) 737-9680 Facsimile: (613) 737-9691 Name and title Date Tested by: Kevin Ma, Wireless/EMC Specialist June 14, 2010 Reviewed by: Andrey Adelberg, Senior Wireless/EMC Specialist June 14, 2010 Nemko Canada Inc., a testing laboratory, is accredited by the Standards Council of Canada. The tests included in this report are within the scope of this accreditation. 15.231.doc - Date: April 13, 2010 Product: Telemedic MUMS-002 Nemko Canada Inc., 303 River Rd, Ottawa, ON, Canada, K1V 1H2 Report reference ID: 146144-1TRFWL Page 2 of 23 Table of contents Section 1: Report summary.........................................................................................................................................................3 1.1 Test specification.........................................................................................................................................................3 1.2 Statement of compliance.............................................................................................................................................3 1.3 Exclusions....................................................................................................................................................................3 1.4 Registration number....................................................................................................................................................3 1.5 Test report revision history...........................................................................................................................................3 1.6 Limits of responsibility..................................................................................................................................................3 Section 2: Summary of test results.............................................................................................................................................4 2.1 FCC Part 15 Subpart C – Intentional Radiators, test results........................................................................................4 Section 3: Equipment under test (EUT) and application details...............................................................................................5 3.1 Applicant details...........................................................................................................................................................5 3.2 Modular equipment......................................................................................................................................................5 3.3 Product details.............................................................................................................................................................5 3.4 Accessories and support equipment............................................................................................................................5 3.5 Application purpose.....................................................................................................................................................6 3.6 Composite/related equipment......................................................................................................................................6 3.7 Sample information......................................................................................................................................................6 3.8 EUT technical specifications........................................................................................................................................6 3.9 Operation of the EUT during testing............................................................................................................................6 3.10 EUT setup diagram......................................................................................................................................................7 Section 4: Engineering considerations.......................................................................................................................................8 4.1 Modifications incorporated in the EUT.........................................................................................................................8 4.2 Deviations from laboratory tests procedures................................................................................................................8 4.3 Technical judgment......................................................................................................................................................8 Section 5: Test conditions...........................................................................................................................................................9 5.1 Power source and ambient temperatures....................................................................................................................9 Section 6: Measurement uncertainty........................................................................................................................................10 Section 7: Test equipment.........................................................................................................................................................11 7.1 Test equipment list......................................................…

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