ISO Packaging Standards

This document specifies the requirements and test methods for external tooth bleaching products. These products are intended for use in the oral cavity, either by professional application (in-office tooth bleaching products) or consumer application (professional or non-professional home use of...

This document is applicable to heart valve substitutes intended for implantation and provides general requirements. Subsequent parts of the ISO 5840 series provide specific requirements. This document is applicable to newly developed and modified heart valve substitutes and to the accessory...

This document specifies the performance requirements for fluxes in solid, liquid and paste forms intended for use with soft solders. NOTE 1 ISO 9454-1 specifies the requirements for labelling and packaging as well as the coding system for the classification of the fluxes. NOTE 2 Some...

This document specifies a procedure for determining whether a perceptible sensory difference or similarity exists between samples of two products. The method is a forced-choice procedure. The method is applicable whether a difference exists in a single sensory attribute or in several attributes....

This document gives guidance on the application of a quality management system in the manufacture, measuring and monitoring of design type approved dangerous goods packaging, intermediate bulk containers (IBCs) and large packaging. This document does not include guidance specific to...

This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of non-critical medical devices not intended to be sterilized (i.e. a medical device that is intended to come into contact with intact skin only or a medical device not...

This document specifies requirements and test methods for hand-held and mechanically operated instruments used for shaping and cleaning root canals, and which are not specified in other parts of the ISO 3630 series. This document specifies requirements for size, marking, product designation,...

This document is applicable to heart valve substitutes intended for implantation in human hearts, generally requiring cardiopulmonary bypass and generally with direct visualization. See Annex E for examples of surgical heart valve substitutes and their components. This document is applicable to...

This document specifies the requirements for the glass cupping device applying negative pressure created by a heat source placed in its inner cavity. This document includes the requirements for configuration, material, performance, packaging and labelling, as well as appropriate test methods...

This document specifies a procedure, in the field of ionizing radiation metrology, for the calculation of the "decision threshold", the "detection limit" and the "limits of the coverage interval" for a non‑negative ionizing radiation measurand when counting measurements with preselection of time or...

This document provides requirements and guidance for methods of Issuer PIN Management using AES. It additionally defines a method for generating and verifying Card Security Codes using AES. The processes defined in this Standard (in order as presented) are: - PIN Generation - PIN Change - PIN...

This document provides requirements and recommendations in designing consumer packages, independent of material, to increase accessibility with regard to handling and manipulation. The document considers packaging needs from a wide range of users with diverse human abilities and needs...

A paragraph. This document establishes the designation, the dimensions, the approved rim contours and the load ratings for 3-part code designated tyres in diagonal or radial construction for lawn, garden tractors and agricultural machines, with a nominal rim diameter code 18 and below.

This document defines the core data set for a patient summary document that supports continuity of care for a person and coordination of their healthcare. It is specifically aimed at supporting the use case' scenario for 'unplanned, cross border care' and is intended to be an international patient...

This document specifies a series of interfaces to allow disparate systems an interoperable management of image repositories. It also specifies the general rules which govern the usage of metadata in JPSearch and provides a specification which - provides rules for the representation of image...

This document gives guidance on methods of handling, mounting and surface treatment for a biomaterial specimen prior to surface chemical analysis. It is intended for the analyst as an aid in understanding the specialized specimen-handling conditions required for analyses by the following...

This document specifies a conceptual schema for locations relative to a one-dimensional object as measurement along (and optionally offset from) that object. It defines a description of the data and operations required to use and support linear referencing. This document is applicable to...