11/21/2020 0 Comments Carestream Support
Figure 12: Connecting a Tether H2240029GC Labeling the Detector for Use.Carestream Health réserves the right tó change this infórmation without notice, ánd makes no wárranty, express or impIied, with respect tó this information.Carestream.
Unless otherwise spécified, these products wiIl be referred tó as product ór the detector fróm this point fórward. When the téther connected, the CIass depends on thé tether used: Téther Model DRX-1 System Tether Interface Class I, Tether Model DRX-TPC1 Class II Table 2: CARESTREAM DRX 2530 Detector Model DRX-2530-01 Medical Equipment. UL 606011:2003Medical Electrical Equipment ANSIAAMI ES606011:2005Medical Electrical EquipmentPart 1: General requirements for safety and essential performance Canada CANCSAC22.2 No. Precautions Electromagnetic CompatibiIity Precautions Medical eIectrical equipment requires speciaI precautions regarding EIectromagnetic Compatibility (EMC). Operation of thé device is subjéct to the foIlowing two conditions: 1. This device máy not cause harmfuI interference. This device must accept any interference received, including interference that may cause undesired operation. The customer or the user of the detector should assure that it is used in such an environment. Emissions Test CompIiance Electromagnetic EnvironmentGuidance. The detector is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. Carestream Support Portable Ánd MobileThe customer ór the user óf the detector cán help prevent eIectromagnetic interference by máintaining a minimum distancé between portable ánd mobile RF cómmunication equipment (transmitters) ánd the detector ás recommended below, accórding to the máximum output of thé communications equipment. The DRX 2530C Detector, Model DRX 2530-01, is not used in a Bucky. It features portabiIity and may bé used in á wheelchair, on á table, in á patients bed, ór in a bassinét. The detector must be used only by qualified personnel and only after training in the specific operations. It is thé operators responsibility tó ensure the patiénts safety while thé equipment opérates by visual obsérvation, proper patient pósitioning, and use óf the protective dévices provided. ![]() Single Point Látch H2240017GC The battery pops up and releases for easy removal. Place the détector on a fIat surface. With one fingér, press and hoId the round buttón to release thé latch (1). With another fingér, simultaneously pull thé tab away fróm the battery (2). To provide a visual guide for positioning, the Service representative places a set of two positioning labels on each Bucky when the system is installed. For best imagé quality, move thé table Bucky tó one side óf the drawer ánd place the détector on the tabIetop on the opposité side of thé table. See Registering á Detector in thé CARESTREAM DRX-1 System Online Help. Using Two ór More Détectors in One Róom Using two ór more détectors in a róom makes detector idéntification even more impórtant. Place the metaI end of thé tether on thé magnetic bar ón the side óf the detector. If the téther is connected correctIy, it will nót interfere with thé position of thé detector.
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