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This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, design, VERIFY and VALIDATE USABILITY, as it relates to BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT, hereafter...

1.1 This Standard is intended to be read together with Annex A, Ref. No. 1. The requirements of Annex A, Ref. No. 1 apply unless modified by this Standard.

.1 This part of ISO/IEC 18000 defines the generic architecture concepts in which item identification may commonly be required within the logistics and supply chain and defines the parameters that need to be determined in any...

These requirements apply to single and multiple jacketed lined fire hose of the following nominal inside diameter trade sizes: 38, 45, 50, 65, 77, 89, 100, 125 and 150 mm (1-1/2, 1-3/4, 2, 2-1/2, 3, 3-1/2, 4, 5, and 6 inch)...

This International Standard applies to the reduction of adverse ENVIRONMENTAL IMPACTS of MEDICAL ELECTRICAL EQUIPMENT, hereafter referred to as ME EQUIPMENT. MEDICAL ELECTRICAL SYSTEMS are excluded from the scope of this...

1.1 This part of ISO/IEC 18000 defines the generic architecture concepts in which item identification may commonly be required within the logistics and supply chain and defines the parameters that need to be determined in any...

This procedure defines the long-term thermal resistance (LTTR) of a foam product as the value measured after 5-year storage in a laboratory environment and provides means for its prediction based on an accelerated laboratory...

This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, design, VERIFY and VALIDATE USABILITY, as it relates to BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT, hereafter...

1.1 This security evaluation standard applies to the testing of network connectable components of healthcare systems. It applies to, but is not limited to, the following key components: a) Medical devices; b) Accessories to...

This Standard is intended to be read together with Annex A, Ref. No. 1. The requirements of Annex A, Ref. No. 1 apply unless modified by this Standard.

1.1 This Standard establishes requirements for door closers intended for use with swinging doors in fire separations and on exit doors. NOTE: Tests in this Standard are performed under laboratory conditions. In actual usage...

This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, design, VERIFY and VALIDATE USABILITY, as it relates to BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT, hereafter...