Datex-Ohmeda $/5™ Light Monitor, F-LM4, F-LMP1 Technical Reference Manual All specifications are subject to change without notice. Document No, 8000060-2 October 2004 GE Healthcare Finland Oy Helsinki, Finland .0. Box 900 F-00031 GE Tel: +358 10 39441, Fax: +3589 1463310 ww. dates-ohmeda.com vwwow.gehealtheare.com © General Electric company. llrightsreserved. Datex-Ohmeda, Inc. P.0. Box 7550, Madison |W153707-7550, USA Tel. 1-608-221-1551 Fax “1-608-222-9147 wuw.us datercohmeda.comIntended purpose Datex-Ohmeda S/5 Light Monitors intended for stationary and mobile monitoring patient's ECS, SpO2, non-invasive and invasive blood pressure, temperature, respiration and CO in hospitals and ambulances. When used outdoor, the monitor must bein the protective case. The monitors intended for use by qualified medical personnel only. The S/5 Light Monitors intended for patients with weight rom 5 kg(11 I.) up. Respiration monitoring is intended for patients three yeas old and up. Classification according to IEC 60601-1 = CLASS EQUIPMENT and INTERNALLY POWERED EQUIPMENT according tothe ype of protection ‘against electical shock. - _TYPEBF or CF equipment according to the degre of protection against electric shocks indicated with ‘a symbol beside each patient connector. Degree of protection against harmful ingress of waters detailed inthe 1EC 60529: Monitor: IPX1, vertically fling water drops shall have no harmful effets (applicable when the monitor isin upright positon, otited backwards). Inthe protective case IPX4, splash proof, when the case is. closed property, the monitoris intact and operates on battery power. Power adapter: IPXO, ordinary equipment. Power adapter fr Transport Vehicles: IPX1. — EQUIPMENT not suitable foruse inthe presence ofa FLAMMABLE ANESTHETIC MIXTURE with air or with oggen or tous oxide, — CONTINUOUS OPERATION according tothe mode of operation. = CISPR 11: Group 1 cass A Classification according to EU Medical Device Directive = The monitoris classified as ib. Responsibility of the manufacturer is responsible for the effects on safety, reliability and performance of the equipment ~ assembly, operations, extensions, readjustments, modifications, service and repairs are caried out by authorized personnel. = the electrical installation ofthe relevant room complies with appropriate requirements. = the equipmentis used in accordance with the User's Reference Manual and serviced and maintained in accordance with the Technical Reference Manual. The C02 measuring option (N-LCM) is manufactured for Instrumentarium Corp. by Pryon Corp., 8500 S.W. Creekside Place, Beaverton, OR 97008-7107 USA. ‘The Nelicor option (N-LNSAT is manufactured for Instrumentarium Corp. by Mallinckrodt Inc., 675 McDonnell Boulevard, P.O. Box 5840, St Louis, MO 63134 USA. Trademarks ‘ComWheel, Datex-Ohmeda S/5, Datex-Ohmeda AS/3, Datex-Ohmeda CS/3, Light, EarSat, FingerSat and Flextite are trademarks of instrumentarium Corp. ‘Storage and transport For allowed storage and transport conditions refer tothe documentation delivered with the monitor. All specifications subject to change without notice. © 2004 General Electric Company. All rights reserved.‘Master table of contents Datex-Ohmeda S/5™ Light Monitor Technical Reference Manual, 8000060-2 PARTI, General Service Guide Dome [oa Dessipton soccoso2 Tandon, ae eee, Fnconal heck, Sere check Gent | 1 trableshooing Sere Meru, Gener spctcatons sovi9a44 PamedWaineranetnaucions | 2 PARTI, Product Service Guide socooeot ou] 4 0000601 Powersippyunt | 2 0000804 Hemodyamicunt | 3 000601 cary [stooees \oaton over Sop UatiercO,unt | § 0201-5 7 Deer OnmedaLgreMantorRecwde,WiREC | 902025 tex Onde ih NontorPoverAdne, POW anawipowt | 7 ss02008 Date Onmede Ligh Menor Batey Wags, FLBAT| 8 961824 Date Ohede Deena Baty Gar vacin | 9 2000000-1 Daal and Nebo Optons MIDATA, NET, WONT | 40 0000601 ‘Spears, Updo KsandBioed we | 14 soesst.a Optonal HL Upgade or tg onto ss22 pona¥ LONE Upgade righ oor 9659.2 Oponaliv DATA Upgrade rig Honor [ cosssa2 Opal NET Upgrade rin Honor ‘Deeumentno.8000060-2