Pregled nacrta

This document specifies the safety requirements and measures for dimension saws (defined in 3.1), capable of continuous production use and hereinafter referred to also as “machines”.
The machines are designed to cut solid wood and material with similar physical characteristics to wood.
This document deals with all significant hazards, hazardous situations and events, listed in Annex A, relevant to the machines, when operated, adjusted and maintained as intended and under the conditions foreseen by the manufacturer; reasonably foreseeable misuse has been considered too. Transport, assembly, dismantling, disabling and scrapping phases have also been taken into account.
This document is also applicable to machines fitted with one or more of the following devices/additional working units, whose hazards have been dealt with:
a)       device to raise and lower the main saw blade and scoring saw blade;
b)       device to tilt the main saw blade and scoring saw blade for angled cutting in one or both directions;
c)        device for scoring;
d)       device for grooving with milling tool with a width not exceeding 20 mm;
e)       demountable power feed unit;
f)         power-operated sliding table;
g)       workpiece clamping.
This document is not applicable to machines intended for use in potentially explosive atmospheres or to machines manufactured prior to the date of its publication.

This document specifies the method for the determination of extractable alkylphenols (AP) without derivatization step in textile and textile products.

ISO 19204:2017 describes in a general way the application of the soil quality TRIAD approach for the site-specific ecological risk assessment of contaminated soils. In detail, it presents in a transparent way three lines of evidence (chemistry, ecotoxicology and ecology) which together allow an efficient, ecologically robust but also practical risk assessment of contaminated soils. This procedure can also be applicable to other stress factors, such as acidification, soil compaction, salinization, loss of soil organic substance, and erosion. However, so far, no experience has been gained with these other applications. Therefore, this document focuses on soils contaminated by chemicals.
NOTE 1       This document focuses on ecological risk assessment. Thus, it does not cover human health end points.
In view of the nature of this document, the investigation procedure is described on a general level. It does not contain details of technical procedures for the actual assessment. However, this document includes references relating to technical standards (e.g. ISO 15799, ISO 17616) which are useful for the actual performance of the three lines of evidence.
In ecological risk assessment, the effects of soil contamination on the ecosystem are related to the intended land use and the requirements that this use sets for properly functioning soil. This document describes the basic steps relating to a coherent tool for a site-specific risk assessment with opportunities to work out site-specific details.
ISO 19204:2017 can also be used for the evaluation of clean-up operations, remediation processes or management measures (i.e. for the evaluation of the environmental quality after having performed such actions).
NOTE 2       This document starts when it has already been decided that an ecological risk assessment at a given site needs to be performed. In other words, the practical performance of the soil quality TRIAD and the evaluation of the individual test results will be described. Thus, nothing will be said about decisions whether (and if yes, how) the results of the assessment are included in soil management measures or not.
NOTE 3       The TRIAD approach can be used for different parts of the environment, but this document focuses mostly on the soil compartment. Comparable documents for other environmental compartments are intended to be prepared in addition (e.g. the terrestrial aboveground compartment) in order to perform a complete site assessment, based on the same principles and processes.

ISO 41012:2017 provides guidance on sourcing and development of agreements in facility management (FM). It highlights:
· essential elements in FM sourcing processes;
· FM roles and responsibilities in sourcing processes;
· development processes and structures of typical agreement models.
ISO 41012:2017 is applicable to:
· strategic processes related to service and support functions for the core business;
· development of FM strategies;
· development of facility service provision agreements covering both public and private service demand and internal and external production/delivery options;
· development of FM information systems;
· FM education and research;
· organization development and business re-engineering processes in major types of working environments (e.g. industrial, commercial, administration, military, healthcare, accommodation).

This document provides a list of removable crimped contacts as specified in the product standards, with wrapped or soldered connections, etc. for use in connectors or other electrical elements of connection. It shows the elements of connection in which they are used.

This document specifies the requirements relating to:

Steel 15CrMoV6 (1.7334)

Air melted

Hardened and tempered

Bars for machining

De ≤ 100 mm

1 080 MPa ≤ Rm ≤ 1 280 MPa

for aerospace applications.

W.nr: 1.7334.

ASD-STAN designation: FE-PL1505.

This document applies to constant-amplitude force-controlled low-cycle fatigue (LCF) testing of metallic materials governed by EN Aerospace standards. The document defines the mechanical properties that need to be determined, the equipment, test pieces, methodology of test and presentation of results.

The document applies to uniaxially loaded tests carried out on plain or notched test pieces under ambient and elevated temperatures. The document does not cover the testing of more complex test pieces, full scale components or structures, although the methodology could well be adopted to provide for such tests.

The purpose of this document is to ensure the comparability and reproducibility of the test results. The document does not cover the evaluation or interpretation of the results.

This document specifies the technical delivery conditions for weldable aluminium alloy plates for armour applications with a nominal thickness between 10 mm and 70 mm for ARAL1 material and between 10 mm and 80 mm for ARAL2 material.

This document specifies requirements for the construction, performance, protective packaging and labelling of Category F4 fireworks, as listed in Clauses 4, 5 and 6.
This document does not apply to fireworks intended to be kept or used at temperatures below −20 °C or above 50 °C.

This document applies to testing of rails installed in track for detecting internal discontinuities.
This part applies to testing equipment fitted to dedicated test vehicles or manually-propelled devices. This document does not define the requirements for vehicle acceptance. This part of the series does not apply to ultrasonic testing of rails in a production plant.
The document specifies the requirements for testing principles and systems in order to produce comparable results with regard to location, type and size of discontinuities in rails. This document is not aiming to give any guidelines for managing the result of ultrasonic rail testing.
This document applies only to rail profiles meeting the requirements of EN 13674 1.

This document specifies a method for extraction, separation, and determination of inorganic arsenic (iAs) in organic or organo-mineral fertilizers using anion-exchange high performance liquid chromatography (HPLC) or ion chromatography (IC) coupled to ICP-MS.
This document is applicable to fertilizing product blends where a blend is a mix of at least two of the following components: fertilizers, liming materials, soil improvers, growing media, inhibitors, plant biostimulants and where the following category organic fertilizer or organo-mineral fertiliser is the highest % in the blend by mass or volume, or in the case of liquid form by dry mass. If the organic fertilizer or the organo-mineral fertilizer is not the highest % in the blend, the European Standard for the highest % of the blend applies. In case a fertilizing product blend is composed of components in equal quantity, the user decides which standard to apply. Variations in analytical methods for fertilizing product blends can lead to differing results as some components or matrix interactions can affect the outcome. Validation procedures have shown that developed standard methods are robust and reliable across diverse product compositions, but possible interferences and unexpected results when analysing fertilizing product blends are possible.

This document provides requirements for the application of basic and well-tried safety principles and conditions for possible fault exclusions.
This document provides guidance for the design and the validation of mechanical, pneumatic, hydraulic, and electrical systems for the safety-related parts of a control system (SRP/CS) designed in accordance with ISO 13849-1:2023.
NOTE Additional requirements for programmable electronic systems, including embedded software, are given in ISO 13849-1:2023, Clause 7, and IEC 61508.

This document addresses symbols that may be used to convey certain items of information related to medical devices dedicated to blood collection processes and storage. The information may be required on the device itself, as part of the label, or provided with the device. Many countries require that their own language be used to display textual information with medical devices. This raises problems to device manufacturers and users.
The symbols specified in this document do not replace current national regulatory requirements.
Manufacturers seek to take costs out of labelling by reducing or rationalizing variants. This results in a major problem of translation, design and logistics when multiple languages are included on a single label or piece of documentation.  As other medical devices, blood medical devices, labelled in a number of different languages, can experience confusion and delay in locating the appropriate language. This document proposes solutions to these problems through the use of internationally recognized symbols with precisely defined meanings.
This document is primarily intended to be used by manufacturers of medical devices dedicated to the blood collection, process storage and distribution, who market identical products in countries having different language requirements for medical device labelling.
This document may also be of assistance to different stages of the blood supply chain, e.g.:

distributors of blood collection devices (manual or automated) or other representatives of manufacturers;
blood centres and distribution centres to simplify and secure the operating procedures.

The use of these symbols is primarily intended for the medical device rather than the therapeutic product.
This document does not specify requirements relating to the size and colour of symbols although the symbols specified have been specially designed so as to be clearly legible when reproduced in the space typically available on the labels of blood treatment and transfusion devices, and also so as to be suitable for on-line printing.
Several of the symbols specified in this document may be suitable for application in other areas of medical technology.

ISO 3826-3:2006 specifies requirements, including performance requirements, for integrated features on plastic, collapsible, non-vented, sterile containers (blood bag systems).
The integrated features refer to:

leucocyte filter;
pre-donation sampling device;
top and bottom bag;
platelet storage bag;
needle stick protection device.

In addition to ISO 3826-1:2003, which specifies the requirements of conventional containers, ISO 3826-3:2006 specifies additional requirements for blood bag systems using multiple units.
Unless otherwise specified, all tests specified in ISO 3826-3:2006 apply to the plastic container as prepared ready for use.

This document specifies requirements including performance requirements for aphaeresis blood bag systems with integrated features. Aphaeresis blood bag systems need not contain all of the integrated features identified in this part of ISO 3826.
The integrated features refer to: needle stick protection device, leucocyte filter, sterile barrier filter, pre-collection sampling device, red blood cell storage bag, plasma storage bag, platelet storage bag, polymorphonucleic (e.g. stem) cell storage bag, post-collection sampling devices, and connections for storage solutions, anticoagulant, and replacement fluid.
This document specifies additional requirements for blood bag systems used to collect varying quantities of blood components or cells by apheresis. It can be used on automated or semi-automated blood collection systems.

This document provides the part of the method to calculate the GHG emissions throughout the
LNG chain specific to shipping.
The general requirements are covered in ISO 6338-1.

This document provides the part of the method to calculate the GHG emissions throughout the
LNG chain specific to regasification.
The general requirements are covered in ISO 6338-1.

This document specifies requirements for qualification testing of brazers and brazing operators for metallic materials.
This document gives general provisions on quality requirements for brazing (see Annex A).
This document applies to the following brazing processes according to ISO 857-2 and ISO 4063:2009 with local and global heating:
—    911 Infrared brazing;
—    912 Flame brazing, torch brazing;
—    913 Laser beam brazing;
—    914 Electron beam brazing;
—    916 Induction brazing;
—    918 Resistance brazing;
—    919 Diffusion brazing;
—    921 Furnace brazing;
—    922 Vacuum brazing;
—    923 Dip-bath brazing;
—    924 Salt-bath brazing;
—    925 Flux bath brazing;
—    926 Immersion brazing;
—    972 Arc weld brazing.
This document is not applicable to personnel operating brazing equipment who do not have any direct influence on the quality of the brazed joint, for example, personnel performing exclusively loading/unloading the brazing unit or just initiating the brazing cycle in automatic brazing.
The principles of this document can be applied to other brazing processes and brazing of materials not listed.
This document does not apply to brazing for aerospace applications covered by ISO 11745.