Pregled nacrta
This part of ISO 8502 describes a field test for the measurement of chloride ions using special detection tubes.
With suitable surface sampling techniques, the test is applicable to steel surfaces before and after cleaning, as well as to painted surfaces between applications of coats.
This document is applicable to all electronic equipment for control, regulation, protection, diagnostic, energy supply, etc. installed on rail vehicles.
For the purpose of this document, electronic equipment is defined as equipment composed of electronic components (e.g. resistors, capacitors, transistors, diodes, integrated circuits, hybrids, application specific integrated circuits, wound components and relays), and recognized associated components (e.g. connectors, mechanical parts). These components are mainly mounted on printed circuit boards.
Sensors (e.g. current, voltage, speed) and semiconductor drive units for power electronic devices are covered by this document. Complete semiconductor drive units and power converters are covered by EN 61287-1.
This document covers the requirements for operating conditions, design, documentation, testing and integration of electronic equipment, as well as hardware and software requirements considered necessary for compliant and reliable equipment.
Specific requirements related to practices necessary to ensure defined safety integrity level or functional safety are not covered by this document. Nevertheless, this document is applicable to the hardware of all rolling stock electronic equipment or systems performing safety-related functions.
The software development requirements for on-board railway equipment are specified by EN 50716.
ISO 284:2012 specifies the maximum electrical resistance of a conveyor belt and the corresponding test method.
The test is intended to ensure that the belt is sufficiently conductive to avoid the accumulation of electrical static charge which can be developed during service use.
ISO 284:2012 is not suitable or applicable to light conveyor belts as described in ISO 21183-1, the static electrical properties of which are measured by ISO 21178.
Provides a method for measuring the time of liquid (simulated urine) strike-through for nonwovens. Does not simulate in-use conditions for finished products.
This document establishes basic principles and specifies requirements and methods to determine cardinal values of bacteria and yeast strains.
These methods are based on (1) the determination of maximum specific growth rates of the studied strain grown in a defined range of values of the intrinsic or extrinsic factor under study and (2) on the use of secondary models to obtain the cardinal values.
These methods can be applied to all type of bacteria and yeasts.
Finally, this document provides guidelines on the use of the determined cardinal values in growth simulation based on predictive microbiological models.
This document specifies the safety requirements and measures for horizontal cutting cross-cut sawing machines with one saw unit (radial arm saws) with manual loading and/or unloading of the workpiece and capable of continuous production use, hereinafter referred to also as “machines”.
This document specifies the safety requirements and measures for double blade circular sawing machines for cross-cutting with integrated feed of the cutting-stroke, with manual loading and/or unloading of the workpiece and capable of continuous production use, hereinafter referred to also as “machines”.
This document specifies the safety requirements and measures for single blade automatic and semi-automatic up-cutting cross-cut sawing machines, capable of continuous production use, hereinafter referred to also as “machines”.
ISO 1120:2012 specifies a static test method for measuring the strength of a conveyor belt mechanical fastening; the mechanical joints can be either of the type employing a connecting rod or of a type which does not employ a connecting rod.
This document specifies test methods for the determination of the plastics compatibility of packaging/intermediate bulk containers (IBC) made from polyethylene, fluorinated polyethylene and coextruded plastics.
It covers the determination of adequate plastics compatibility against the processes of deterioration:
- softening due to absorption (swelling);
- stress cracking; and
- combinations thereof.
It applies to:
- drums and containers made from plastics according to paragraph 6.1.4.8 of the UN recommendations 1);
- composite packaging (plastics) with inner receptacle made from plastics according to paragraph 6.1.4.19 of the UN recommendations;
- rigid plastics IBCs (types 31H1 and 31H2) according to 6.5.5.3 of the UN recommendations; and
- composite IBCs with rigid plastics inner receptacles (type 31HZ1) according to 6.5.5.4 of the UN recommendations;
whose design is approved by a competent authority for the transport of liquid dangerous goods.
This proof of adequate plastics compatibility is only applicable to the above packaging and IBC types of the following materials and material specifications:
- packaging and IBCs made from polyethylene (PE);
- packaging and IBCs made from polyethylene (PE), whose internal surfaces are fluorinated; and
- packaging and IBCs which are coextrusion blow moulded and have walls with the following multilayer structure (from inside to outside):
- polyamide (PA)//bonding agents//polyethylene (PE); or
- ethyl vinyl alcohol (EVOH)//bonding agents//polyethylene (PE).
1) UN Recommendations on the Transport of Dangerous Goods – Model Regulations
This document specifies the requirements for the tensile testing of metallic materials at ambient temperature for aerospace applications.
It is applied when referred to in the EN technical specification or material standard unless otherwise specified on the drawing, order or inspection schedule.
This document specifies the requirements for the tensile testing of metallic materials at elevated temperature for aerospace applications.
It is applied when referred to in the EN technical specification or material standard unless otherwise specified on the drawing, order or inspection schedule.
This document specifies the female coding and attachment system for mounting on free housing in the family of rectangular electrical connectors with sealed and non-sealed rear, plastic housing, locking device, for operating temperatures from -55 °C to 175 °C.
This document specifies the characteristics of multilayer mechanical locked floor covering with a wear-resistant and decorative surface layer supplied in panels (either tile or plank form). The floor panels are considered suitable for domestic and commercial levels of use and designed for floating installation.
This document does not apply to resilient floor panels for loose-laying according to EN ISO 20326, to multilayer wood floorings according to EN 13489, to wood veneer floor coverings according to EN 14354, to laminate floor covering according to EN 13329, EN 14978 and EN 15468 nor to products specified in EN ISO 10581, EN ISO 10582, EN ISO 24011, EN 12104 and ISO 14486.
This document is applicable to areas which are subject to frequent wetting, e.g. bathrooms, laundry rooms or saunas, only if specified by the producer.
This document also includes requirements for marking and packaging.
In Annex A (informative), optional properties are given. In Annex B (informative), a test method for the classification of the flexibility is given.
ISO 15715:2003 specifies an instrumental method for determining the turbidity of clear liquids. It is applicable to resins and resin solutions, solvents, clear coating materials, monomers and any other liquids where clarity is specified.
This document is applicable to the basic safety and essential performance of oxygen conserving equipment, hereafter referred to as ME equipment, in combination with its accessories intended to conserve supplemental oxygen by delivering gas intermittently and synchronized with the patient's inspiratory cycle, when used in the home healthcare environment. Oxygen conserving equipment is typically used by a lay operator.
NOTE 1 Conserving equipment can also be used in professional health care facilities.
This document is also applicable to conserving equipment that is incorporated with other equipment.
EXAMPLE Conserving equipment combined with a pressure regulator[2], an oxygen concentrator[7] or liquid oxygen equipment[4].
This document is also applicable to those accessories intended by their manufacturer to be connected to conserving equipment, where the characteristics of those accessories can affect the basic safety or essential performance of the conserving equipment.
This document is intended to clarify the difference in operation of various conserving equipment models, as well as between the operation of conserving equipment and continuous flow oxygen equipment, by requiring standardized performance testing and labelling.
This document is only applicable to active devices (e.g. pneumatically or electrically powered) and is not applicable to non-active devices (e.g. reservoir cannulas).
If a clause or subclause is specifically intended to be applicable to ME equipment only, or to ME systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME equipment and to ME systems, as relevant.
Hazards inherent in the intended physiological function of ME equipment or ME systems within the scope of this document are not covered by specific requirements in this document except in IEC 60601-1:2005+AMD1:2012, 7.2.13 and 8.4.1.
NOTE 2 Additional information can be found in IEC 60601-1:2005+AMD1:2012, 4.2.
This document specifies requirements for the basic safety and essential performance of an oxygen concentrator in combination with its accessories, hereafter referred to as ME equipment, intended to increase the oxygen concentration of gas intended to be delivered to a single patient. Such oxygen concentrators are typically intended for use in the home healthcare environment by a single patient in various environments including any private and public transportation as well as in commercial aircraft.
NOTE 1 Such oxygen concentrators can also be used in professional healthcare facilities.
This document is applicable to a transit-operable and non-transit-operable oxygen concentrator. This document is applicable to an oxygen concentrator integrated into or used with other medical devices, ME equipment or ME systems.
EXAMPLE 1 An oxygen concentrator with integrated oxygen conserving equipment function or humidifier function.
EXAMPLE 2 An oxygen concentrator used with a flowmeter stand.
EXAMPLE 3 An oxygen concentrator as part of an anaesthetic system for use in areas with limited logistical supplies of electricity and anaesthetic gases[2].
EXAMPLE 4 An oxygen concentrator with an integrated liquid reservoir function or gas cylinder filling system function.
This document is also applicable to those accessories intended by their manufacturer to be connected to an oxygen concentrator, where the characteristics of those accessories can affect the basic safety or essential performance of the oxygen concentrator.
NOTE 2 Such accessories can include, but are not limited to, masks, cannulae, extension tubing, humidifiers, carts, carrying cases, external power sources and oxygen conserving equipment.
This document does not specify requirements for oxygen concentrators for use with a medical gas pipeline system.
If a clause or subclause is specifically intended to be applicable to ME equipment only, or to ME systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME equipment and to ME systems, as relevant.
Hazards inherent in the intended physiological function of ME equipment or ME systems within the scope of this document are not covered by specific requirements in this document except in 7.2.13 and 8.4.1 of the general standard.
NOTE 3 See also 4.2 of the general standard.
ISO 13802:2015 specifies frequency and methods for the verification of pendulum impact-testing machines used for the Charpy impact test, Izod impact test, and tensile impact test described in ISO 179‑1, ISO 180, and ISO 8256, respectively. Verification of instrumented impact machines is covered insofar as the geometrical and physical properties of instrumented machines are identical to non instrumented machines. The force/work verification of instrumented machines is not covered in this International Standard.