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1. Scope 1.1 This Standard sets forth criteria for determining the need for a routine environmental monitoring program. 1.2 This Standard provides guidelines for establishing an environ mental program covering (a) sampling and analysis protocols;

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CSA Preface This is the first edition of CAN/CSA-C22.2 No. 60601-2-49, Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment, which is an adoption without modification of the iden

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CSA Preface This is the second edition of CAN/CSA-C22.2 No. 60601-2-34, Medical electrical equipment - Part 2-34: Particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment, which is an adop

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1.1 Scope Addition: This Particular Standard specifies particular safety requirements for ULTRASONIC DIAGNOSTIC EQUIPMENT as defined in 2.1.145. This standard does not cover ultrasonic therapeutic equipment; however, equipment used for the imaging

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Amendment 1:2005 to CAN/CSA-C22.2 No. 60601-2-37-03, Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment

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1. Scope 1.1 At the onset of an accident, certain protective actions (e.g., reactor trip, emergency core cooling actuation, containment isolation) are designed to be performed automatically. Specific CSA Standards cover the systems that perform these

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CSA Preface This is the first edition of CAN/CSA-ISO 14064-2, Greenhouse gases - Part 2: Specification with guidance at the project level for quantification, monitoring and reporting of greenhouse gas emission reductions or removal enhancements, which

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CSA Preface This is the first edition of CAN/CSA-ISO 15197, In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus, which is an adoption without modification of the identicall

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1.1 Scope ISO 7767 is one of a series of International Standards based on IEC 601-1 (the "General Standard"). This type of International Standard is referred to as a "Particular Standard". As stated in 1.3 of IEC 601-1:1988, the requirements of this I

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1.1 Scope This Standard specifies the particular safety requirements for ELECTROCARDIOGRAPHIC (ECG) MONITORING EQUIPMENT as defined in 2.101 and hereinafter also referred to as EQUIPMENT. Telemetry monitors, ambulatory ("Holter") monitors and other

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Z364.2.1-94 (R2001) Fluid Supply and Monitoring Systems for Haemodialysis 现行 发布日期 :  1970-01-01 实施日期 : 

1. Scope 1.1 General This Standard applies to (a) reagents and apparatus for preparing dialysing fluid; (b) monitors of the dialysing fluid; (c) accessories for monitoring the extracorporeal blood circuit; and (d) blood pumps, infusion, and single

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1 Scope and object This clause of the General Standard applies except as follows: 1.1 Scope Addition: This Particular Standard specifies requirements for the safety, including essential performance, of TRANSCUTANEOUS PARTIAL PRESSURE MONITORING E

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Scope and object This clause of the General Standard applies except as follows: 1.1 Scope Addition: This Particular Standard specifies requirements for the safety, including essential performance, of AUTOMATIC CYCLING NON-INVASIVE BLOOD PRESSUR

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