Self-propelled machinery for forestry — Roll-over protective structures — Laboratory tests and perfo...
ISO 8082:2003 establishes a consistent, reproducible means of evaluating the force-deflection characteristics of roll-over protective structures (ROPS) on self-propelled forestry machines under static loading, and prescribes performance requirements for a representative specimen under such loading. It is applicable to forwarders, skidders, feller-bunchers, processors, harvesters and loaders, as…
ISO 5007:2003 specifies, in accordance with ISO 10326-1, a laboratory method for measuring and evaluating the effectiveness of the suspension of operator seats on agricultural wheeled tractors. It also specifies acceptance criteria based on the test results, while defining the input spectral classes relating to three classes of agricultural tractor with rubber tyres, unsprung rear axles and no…
Health informatics — Clinical analyser interfaces to laboratory information systems — Use profiles
ISO 18812:2003 specifies general messages for electronic information exchange between analytical instruments (AIs) and laboratory information systems (LISs) within a clinical laboratory. It is applicable to the specialities of clinical chemistry/biochemistry, haematology, toxicology, microbiology, virology and immunology. It is not applicable to the blood transfusion and blood bank speciality…
ISO 14233:2003 gives compositional, performance, user-information, packaging and marking, and testing requirements for polymer-based die materials used in dentistry. It is applicable to die materials having a polymeric matrix as their principal constituent. Polymer-based die materials are used in the dental laboratory mainly to produce casts from dental impressions for the manufacture of fixed or…
Industrial automation systems and integration — Open systems application integration framework — Par...
ISO 15745 defines an application integration framework - a set of elements and rules for describing integration models and application interoperability profiles.
ISO 15745-1:2003 defines the generic elements and rules for describing integration models and application interoperability profiles, together with their component profiles - process profiles, information exchange profiles, and resource…
Workplace atmospheres — Controlling and characterizing errors in weighing collected aerosols
ISO 15767:2003 provides recommendations for controlling the analytical uncertainty associated with aerosol collection medium instability, where collection medium or substrate includes any article used to collect particles (e.g. filter or foam material) as well as those supporting elements which must be analysed by weighing.
ISO 15767:2003 is applicable to results compiled both from the literature…
METHOD OF TEST FOR SURFACE BURNING CHARACTERISTICS
OF FLOORING, FLOOR COVERINGS, AND MISCELLANEOUS ...
1. SCOPE
1.1 This method is applicable to the finished surface or covering of a floor extending
to a maximum depth of 65 mm. It may also be applied to materials that cannot conveniently be
tested in a ceiling mounted configuration. Thermoplastic and loose fill materials might be
included in this category.
1.2 The primary purpose of the test is to determine the comparative burning…
METHOD OF TEST FOR SURFACE BURNING CHARACTERISTICS
OF BUILDING MATERIALS AND ASSEMBLIES
1. SCOPE
1.1 This method of test for surface burning characteristics of building materials is
applicable to any type of building material that, by its own structural qualities or the manner in
which it is applied, is capable of supporting itself in position or may be supported in the test
furnace to a thickness comparable to its recommended use.
NOTE: For materials which cannot be so…
Packaging for terminally sterilized medical devices
This International Standard specifies the requirements for single-use materials and reusable containers used for packaging of terminally sterilized medical devices, whether produced industrially or in health care facilities.
This International Standard outlines principal requirements for packaging process development and validation for the manufacturer of terminally sterilized medical devices.…