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This standard sets forth requirements to maintain and enhance the safety, efficacy, and quality of blood collection, storage, processing, and transfusion. This Standard includes requirements for transfusion services that...

IEC 62304:2006+A1:2015 Defines the life cycle requirements for medical device software. The set of processes, activities, and tasks described in this standard establishes a common framework for medical device software life...

Provide guidance on the manufacture, sale and use of barbecue brushes, including metal bristle brushes; and define the characteristics of the tool, and include minimum specifications for materials, construction, labelling and...

This Standard describes methods for the preparation of low-basis weight handsheets of cellulose filaments (CF) and CF-reinforced pulp handsheets to be used for physical testing. This Standard also covers the preparation of...

This part of ISO/IEC 9314 specifies a series of tests in order to verify conformance of FDDI stations to the requirements of ISO/IEC 9314-3:1990. NOTE: ISO/IEC 9314-3 specifies the requirements for the optical input/output...

This Recommendation | International Standard defines the ITU-T programming language CHILL. When CHILL was first defined in 1980 "CHILL" stood for CCITT High Level Language. The following subclauses of this clause introduce...

This document specifies the particular requirements, including performance criteria for washer-disinfectors (WD) that are intended to be used for cleaning and chemical disinfection of thermolabile endoscopes. This document...

specifies requirements and provides guidance on the enumeration and microbial characterization of the population of viable microorganisms on or in a health care product, component, raw material or package

specifies general performance requirements for washer-disinfectors (WD) and their accessories that are intended to be used for cleaning and disinfection of re-usable medical devices and other articles used in the context of...

Defines terms in the field of the sterilization of health care products including related equipment and processes.

specifies requirements for the development, validation and routine control of a dry heat sterilization process for medical devices. It also specifies requirements and provides guidance in relation to depyrogenation processes...

ISO/IEC 15938-6:2003 is the reference software for ISO/IEC 15938 standard. It implements the normative components of the ISO/IEC 15938 standard, which are the descriptors and description schemes and their coding schemes...