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PURPOSE AND SCOPE This standard specifies the test method used to determine the in-place density of soil using a plastic rubber elastic membrane (Washington type apparatus). However, this test cannot be used on soil which...

IEC 60601-2-2:2017 applies to the basic safety and essential performance of HF surgical equipment and HF surgical accessories. HF surgical equipment having a rated output power not exceeding 50 W (for example for micro...

This International Standard specifies general and safety requirements for light-emitting diode (LED) modules: LED modules without integral control gear for operation under constant voltage, constant current or constant power...

This standard applies to three types of middle distillate fuel oils that are suitable for use in liquid-fuel-burning equipment without preheating (Types 0, 1 and 2), and three types of fuel oils that contain residual fuel...

The primary purpose of the multipart standard ISO/IEC 19763 is to specify a metamodel framework for interoperability. This part of ISO/IEC 19763 specifies a metamodel for registering models of services, facilitating...

Note: As requested by the responsible SDO, this NOI being reissued as the standard was in the initial stages of development for more than 12 months. An additional comment period of August 15 to September 6, 2023 (originally...

This part of International Standard ISO/IEC 9075 specifies the syntax and semantics of a database language for declaring and maintaining persistent database language routines in SQL-server modules. The database language for s...

1. Scope 1.1 Equipment covered This part of IEC 60950 applies to information technology equipment intended to be installed in an OUTDOOR LOCATION. The requirements for OUTDOOR EQUIPMENT also apply, where relevant, to empty...

This part of International Standard ISO/IEC 9075 specifies the syntax and semantics of a database language for declaring and maintaining persistent database language routines in SQL-server modules. The database language for s...

This Standard addresses the safe, effective, and reliable reprocessing of reusable medical devices at each phase of the reprocessing workflow and it provides MDR specific requirements for QMS, personnel, MIFUs, purchase and...

1 General NOTE - This Part is intended to be read together with the Standard for Low-Voltage Fuses - Part 1: General Requirements, hereafter referred to as Part 1. The numbering of the Clauses in this Part corresponds to like...

1 General NOTE - This Part is intended to be read together with the Standard for Low-Voltage Fuses - Part 1: General Requirements, hereafter referred to as Part 1. The numbering of the Clauses in this Part corresponds to like...