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 components
and require preheating (Types 4, 5 and 6).
The heating fuel oils covered by this standard are intended for use in oil burning equipment to generate heat for…
This standard applies to two types of diesel fuel, Type A and Type B, suitable for use in high-speed diesel engine
powered equipment for on-road and off-road applications and in select equipment powered by medium speed diesel
engines.
Type A is intended for use in selected applications such as urban buses and underground mining or when ambient
temperatures require better low-temperature…
Diesel fuel containing low levels of biodiesel (B1–B5)
This standard applies to two types of diesel fuel, Type A, Bx and Type B, Bx, suitable for use in high-speed diesel
engine powered equipment for on-road and off-road applications and in select equipment powered by medium
speed diesel engines.
Bx represents biodiesel fuel containing x percent by volume of biodiesel component in the range of 1.0 to 5.
Type A, Bx is intended for use in selected…
This standard applies to Type B, Bxx diesel fuel containing from 6% to 20% by volume of biodiesel. Fuel to this
standard is intended for use in high-speed diesel powered equipment for on-road and off-road applications and in
select equipment powered by medium-speed diesel engines.
Users of fuel meeting this standard are advised to refer to the owner’s manual of their vehicle, engine or…
Biodiesel (B100) for blending in middle distillate fuels
This standard applies to one grade of biodiesel that is intended for use as a blending component in middle distillate
fuels.
Biodiesel meeting this standard is not intended for use as a fuel in its neat form.
See Annex B for regulations that apply to diesel fuels.
The testing and evaluation of a product against this standard may require the use of materials and/or equipment
that could be…
Document management — Electronically stored information — Recommendations for trustworthiness and re...
ISO/TR 15801:2017 describes the implementation and operation of information management systems that store and make available for use electronically stored information (ESI) in a trustworthy and reliable manner. Such ESI can be of any type, including "page based" information, information in databases and audio/video information.
ISO/TR 15801:2017 is for use by any organization that uses…
This standard applies to sealed insulating glass (IG) units used in windows, doors and curtain walls in building
envelopes. It includes requirements for the testing of samples for the integrity and durability of the unit’s hermetic
seal and if applicable, gas concentration.
The requirements contained herein are applicable to glass units consisting of two or three sheets of glass and
glazed in…
Welding for aerospace applications — Visual inspection of welds
ISO 19828:2017 specifies the requirements for visual inspection of welds in metallic materials and requirements for qualification and certification of personnel for visual weld inspection.
ISO 19828:2017 is also applicable to the visual inspection of the joint prior to or between welding sequences, and of brazed joints. In this case, the contents of theoretical and practical training will need to…
Information technology — Telecommunications cabling requirements for remote powering of terminal equ...
ISO/IEC 29125:2017(E) This document specifies the use of generic balanced cabling for customer premises, as specified in the ISO/IEC 11801 series, for remote powering of terminal equipment. It provides guidance on new cabling installations and renovations. The customer premises may encompass one of more buildings or may be within a building that contains more than one organization. The cabling…
Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood
ISO 10993-4:2017 specifies general requirements for evaluating the interactions of medical devices with blood.
It describes
a) a classification of medical devices that are intended for use in contact with blood, based on the intended use and duration of contact as defined in ISO 10993‑1,
b) the fundamental principles governing the evaluation of the interaction of devices with blood,
c)…