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This standard specifies the information to be provided by the medical device manufacturer on the processing of medical devices claimed to be re-sterilizable and medical devices intended to be sterilized by the processor. This...

This Standard specifies general and safety requirements for starting devices (starters and ignitors) for tubular fluorescent and other discharge lamps for use on a.c. supplies up to 1 000 V at 50 Hz or 60 Hz which produce...

This document defines the crypto suite for SPECK for the ISO/IEC 18000 air interfaces standards for radio frequency identification (RFID) devices. Its purpose is to provide a common crypto suite for security for RFID devices...

This Standard is applicable to devices for surge protection against indirect and direct effects of lightning or other transient overvoltages. These devices are designed to be connected to the d.c. side of photovoltaic...

This European Standard specifies the requirements and recommendations regarding the healthcare provision, facilities and equipment, education, and ethical framework for the good practice of osteopathy.

This particular standard specifies the requirements for the safety of SHORT-WAVE THERAPY EQUIPMENT, hereafter referred to as ME EQUIPMENT, as defined in subclause 201.3.206.

This document is the base standard for a number of other standards dealing with water treatment equipment, water, dialysis water, concentrates, and dialysis fluid (ISO 23500 series) and provides dialysis practitioners with...

This part of ISO/IEC 7816 specifies security related interindustry commands to be used for personal verification with biometric methods in integrated circuit(s) cards. It also defines the data structure and data access...

Clause 1 of the general standard1) applies, except as follows: 201.1.1 Scope Replacement: This particular standard specifies safety requirements for OPERATING TABLES, whether or not having electrical parts, including...

This part of ISO/IEC 13719 specifies PCTE in abstract, programming-language-independent, terms. It specifies the interface supported by any conforming implementation as a set of abstract operation specifications, together...

This Standard provides test procedures for determining the performance of packaged, self-contained or factory matched hydrogen generation systems with a capacity less than 400 m 3 /h at 0 °C and 101,325 kPa, referred to as...

Scope This standard applies to the safety of MEDICAL ELECTRICAL SYSTEMS, as defined in 2.201. It describes the safety requirements necessary to provide protection for the PATIENT, the OPERATOR and surroundings.