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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.

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)...

.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...

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 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...

These requirements cover the construction and operation of water-based automatic extinguisher units intended for total flooding applications when installed, inspected, tested, and maintained in accordance with the...

These requirements cover components intended for use in the manufacturer of personal flotation devices. Compliance with these requirements does not indicate that the product is intended for use as a component of an end...

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 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...

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 Scope 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)...