iTeh StandardsiTeh Standards
EURUSD
Your shopping cart is empty.
CEN

EN 1500:1997

(Main)

Chemical disinfectants and antiseptics - Hygienic handrub - Test method and requirements (phase 2/step 2)

Chemical disinfectants and antiseptics - Hygienic handrub - Test method and requirements (phase 2/step 2)

This European Standard specifies a method of test simulating practical conditions for establishing whether a product for hygienic handrub reduces the release of transient flora according to requirements when rubbed onto the artificially contaminated hands of volunteers. This European Standard applies to products for hygienic handrub for use in areas and situations where disinfection is medically indicated.

Chemische Desinfektionsmittel und Antiseptika - Hygienische Händedesinfektion - Prüfverfahren und Anforderungen (Phase 2/Stufe 2)

Diese Europäische Norm beschreibt ein Prüfverfahren, das praktische Bedingungen simuliert und festlegt, ob ein zu prüfendes Produkt für die hygienische Händedesinfektion die Abgabe der transienten Flora entsprechend denAnforderungen verringert, wenn es auf den künstlich kontaminierten Händen von freiwilligen Probanden verrieben wird. Die Europäische Norm bezieht sich auf Produkte zur hygienischen Händedesinfektion, die in Bereichen und unter Bedingungen angewendet werden, wo eine Desinfektion medizinisch angezeigt ist.

Antiseptiques et désinfectants chimiques - Traitement hygiénique des mains par frictions - Méthode d'essai et prescriptions (phase 2/étape 2)

Cette norme européenne décrit une méthode d'essai simulant des conditions pratiques afin d'établir si une préparation pour le traitement hygiénique des mains réduit la flore transitoire conformément aux exigences lorsqu'elle est utilisée en frictions sur les mains artificiellement contaminées de volontaires.Cette norme européenne s'applique aux produits destinés au traitement hygiéniquedes mains par frictions dans les zones et les situations où la désinfection est médicalement préconisée.

Kemična razkužila in antiseptiki - Higiensko razkuževanje rok - Preskusna metoda in zahteve (faza 2/stopnja 2)

General Information

Status
Withdrawn
Publication Date
22-Jul-1997
Withdrawal Date
23-Apr-2013
ICS
11.080 - Sterilization and disinfection
Technical Committee
CEN/TC 216 - Chemical disinfectants and antiseptics
Drafting Committee
CEN/TC 216/WG 1 - Human medicine
Current Stage
9960 - Withdrawal effective - Withdrawal
Start Date
24-Apr-2013
Completion Date
24-Apr-2013
Ref Project
SIST EN 1500:2001 - Chemical disinfectants and antiseptics - Hygienic handrub - Test method and requirements (phase 2/step 2)

Relations

Replaced By
EN 1500:2013 - Chemical disinfectants and antiseptics - Hygienic handrub - Test method and requirements (phase 2/step 2)
Effective Date
22-Dec-2008

Buy Standard

EN 1500:2001EN 1500:2001
PreviousNext
Standard
EN 1500:2001
English language
22 pages
sale 10% off
Preview
sale 10% off
Preview
e-Library read for
1 day

Standards Content (Sample)

2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Chemische Desinfektionsmittel und Antiseptika - Hygienische Händedesinfektion - Prüfverfahren und Anforderungen (Phase 2/Stufe 2)Antiseptiques et désinfectants chimiques - Traitement hygiénique des mains par frictions - Méthode d'essai et prescriptions (phase 2/étape 2)Chemical disinfectants and antiseptics - Hygienic handrub - Test method and requirements (phase 2/step 2)71.100.35Kemikalije za dezinfekcijo v industriji in domaChemicals for industrial and domestic disinfection purposes11.080.20Dezinfektanti in antiseptik
...

Questions, Comments and Discussion

Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.

This May Also Interest You

CEN
EN 1500:2013(Main)
Chemical disinfectants and antiseptics - Hygienic handrub - Test method and requirements (phase 2/step 2)
SIST EN 1500:2013

This European Standard specifies a test method simulating practical conditions for establishing whether a product for hygienic handrub reduces the release of transient microbial flora on hands when rubbed onto the artificially contaminated hands of volunteers.
NOTE 1   Attention is drawn to the fact that tests on human volunteers are the subject of legal provisions in certain European countries/regions.
This European Standard applies to products for hygienic handrub for use in areas and situations where disinfection is medically indicated. Such indications occur in patient care, for example:
- in hospitals, in community medical facilities and in dental institutions,
- in clinics of schools, of kindergartens and of nursing homes;
and may occur in the workplace and in the home. It may also include services such as laundries and kitchens supplying products directly for the patient.
EN 14885 specifies in detail the relationship of the various tests to one another and to "use recommendations".
NOTE 2   This method corresponds to a phase 2, step 2 test.

  • Standard
    37 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN 1499:2013(Main)
Chemical disinfectants and antiseptics - Hygienic handwash - Test method and requirements (phase 2/step 2)
SIST EN 1499:2013

This European Standard specifies a test method simulating practical conditions for establishing whether a product for hygienic handwash reduces the release of transient microbial flora on hands when used to wash the artificially contaminated hands of volunteers.
NOTE 1   Attention is drawn to the fact that tests on human volunteers are the subject of legal provisions in certain European countries/regions.
This European Standard applies to products for hygienic handwash for use in areas and situations where disinfection is medically indicated. Such indications occur in patient care, for example:
- in hospitals, in community medical facilities and in dental institutions,
- in clinics of schools, of kindergartens and of nursing homes;
and may occur in the workplace and in the home. It may also include services such as laundries and kitchens supplying products directly for the patient.
EN 14885 specifies in detail the relationship of the various tests to one another and to "use recommendations".
NOTE 2   This method corresponds to a phase 2, step 2 test.

  • Standard
    32 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN 1422:2014(Main)
Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
SIST EN 1422:2014

This European Standard specifies the requirements and the relevant tests for automatically controlled sterilizers employing ethylene oxide (EO) gas as the sterilant, either as a pure gas or a mixture with other gases, being used for the sterilization of medical devices and their accessories.
This European Standard specifies requirements for ethylene oxide sterilizers (EO-sterilizers) working at super or sub-atmospheric pressure for:
- the performance and design of sterilizers to ensure that the process is capable of sterilizing medical devices;
- the equipment and controls of these sterilizers necessary for the validation and routine control of the sterilization processes.
The test loads described in this European Standard are selected to represent a number of loads for the evaluation of the performance of EO sterilizers for medical devices. However, specific loads may require the use of other test loads.
This European Standard does not specify those tests which are necessary to determine the probability of a processed product being sterile, nor the routine quality control tests required prior to release of sterile product. These topics are addressed in prEN ISO 11135:2012.
This European Standard does not specify requirements for occupational safety associated with the design and operation of EO sterilization facilities.
NOTE 1   For further information on safety, see examples in the Bibliography. National or regional regulations can exist.
This European Standard does not cover sterilizers which employ the injection of EO or mixtures containing EO directly into packages or into a flexible chamber.
NOTE 2   See EN ISO 14937.
This European Standard is not intended as a checklist for suitability of an existing EO sterilizer when assessing compliance with prEN ISO 11135:2012. This standard is not intended to be applied retrospectively.
This European Standard does not cover analytical methods for determining levels of residual EO and/or its reaction products.
NOTE 3   For further information see ISO 10993 7.

  • Standard
    49 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN 1500:2013(Main)
Chemical disinfectants and antiseptics - Hygienic handrub - Test method and requirements (phase 2/step 2)
SIST EN 1500:2013

This European Standard specifies a test method simulating practical conditions for establishing whether a product for hygienic handrub reduces the release of transient microbial flora on hands when rubbed onto the artificially contaminated hands of volunteers.
NOTE 1   Attention is drawn to the fact that tests on human volunteers are the subject of legal provisions in certain European countries/regions.
This European Standard applies to products for hygienic handrub for use in areas and situations where disinfection is medically indicated. Such indications occur in patient care, for example:
- in hospitals, in community medical facilities and in dental institutions,
- in clinics of schools, of kindergartens and of nursing homes;
and may occur in the workplace and in the home. It may also include services such as laundries and kitchens supplying products directly for the patient.
EN 14885 specifies in detail the relationship of the various tests to one another and to "use recommendations".
NOTE 2   This method corresponds to a phase 2, step 2 test.

  • Standard
    37 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN 1499:2013(Main)
Chemical disinfectants and antiseptics - Hygienic handwash - Test method and requirements (phase 2/step 2)
SIST EN 1499:2013

This European Standard specifies a test method simulating practical conditions for establishing whether a product for hygienic handwash reduces the release of transient microbial flora on hands when used to wash the artificially contaminated hands of volunteers.
NOTE 1   Attention is drawn to the fact that tests on human volunteers are the subject of legal provisions in certain European countries/regions.
This European Standard applies to products for hygienic handwash for use in areas and situations where disinfection is medically indicated. Such indications occur in patient care, for example:
- in hospitals, in community medical facilities and in dental institutions,
- in clinics of schools, of kindergartens and of nursing homes;
and may occur in the workplace and in the home. It may also include services such as laundries and kitchens supplying products directly for the patient.
EN 14885 specifies in detail the relationship of the various tests to one another and to "use recommendations".
NOTE 2   This method corresponds to a phase 2, step 2 test.

  • Standard
    32 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN 12347:1998(Main)
Biotechnology - Performance criteria for steam sterilizers and autoclaves
SIST EN 12347:1999

This European Standard specifies performance criteria for steam sterilizer and autoclave used for the destruction and prevention of release of microorganisms used in biotechnological processes. This European Standard applies if the intended use of steam sterilizers or autoclaves includes hazardous or potentially hazardous microorganisms used in biotechological processes or if exposure of the worker or the environment to such microorganisms is restricted for reasons of safety.

  • Standard
    13 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN 1422:1997/prA1(Amendment)
Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
SIST EN 1422:2000/kprA1:2009
  • Draft
    6 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO 16739-1:2024(Main)
Industry Foundation Classes (IFC) for data sharing in the construction and facility management industries - Part 1: Data schema (ISO 16739-1:2024)
kSIST FprEN ISO 16739-1:2024

This document represents an open international standard for information used in Building Information Modeling (BIM) that is exchanged and shared among software applications used by the various participants in the construction or facility management industry sector. This document includes definitions that cover information required for buildings and infrastructure works over their life cycle. This edition of the document added coverage of information required for infrastructure facilities including bridges, roads, railways, waterways and port facilities.
This document comprises the publication of a data schema, its documentation, the property and quantity set definitions and the mechanism of an exchange file format structure.
Definitions from this document are used to support different recognized work flows in the construction and facility management industry sector, representing information deliveries. Such information deliveries can be described according to ISO 29481.
Different implementation levels of this document can be defined to better support multiple information deliveries, they are referred to as a Model View Definition (MVD). Each MVD identifies which subset of the definitions of this document imposes requirements for implementation in software applications. Conforming software applications need to identify the model view definition they conform to when applying for software certification.
The following are within the scope of this edition of this document:
BIM exchange format definitions that are required during the life cycle phases of buildings and infrastructure:
demonstrating the need;
conception of need;
outline feasibility;
substantive feasibility study and outline financial authority;
outline conceptual design;
full conceptual design;
coordinated design;
procurement and full financial authority;
production information;
construction;
operation and maintenance.
BIM exchange format definitions that are required by the various disciplines involved within the life cycle phases:
architecture and civil engineering design;
service and utilities engineering;
structural engineering;
procurement;
construction planning;
facility and utility management;
project management;
client requirement management;
industry authorities for permits and approval.
BIM exchange format definitions including:
project structure;
physical components;
spatial components;
analysis items;
processes;
resources;
controls;
actors;
context definition.

  • Draft
    406 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO 17294-1:2024(Main)
Water quality - Application of inductively coupled plasma mass spectrometry (ICP-MS) - Part 1: General requirements (ISO 17294-1:2024)
kSIST FprEN ISO 17294-1:2023

This document specifies the principles of inductively coupled plasma mass spectrometry (ICP-MS) and provides general requirements for the use of this technique to determine elements in water, digests of sludges and sediments (e.g. digests of water as described in ISO 15587-1 or ISO 15587-2). Generally, the measurement is carried out in water, but gases, vapours or fine particulate matter can be introduced too. This document applies to the use of ICP-MS for aqueous solution analysis.
The ultimate determination of the elements is described in a separate International Standard for each series of elements and matrix. The individual clauses of this document refer the user to these guidelines for the basic principles of the method and the configuration of the instrument.

  • Draft
    43 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO 22435:2024(Main)
Gas cylinders - Cylinder valves with integrated pressure regulators - Specification and type testing (ISO 22435:2024)
kSIST FprEN ISO 22435:2024

This document specifies design, type test methods, marking and instruction requirements for cylinder valves with integrated pressure regulators (VIPRs) intended to be fitted to gas cylinders, pressure drums or tubes or used as a main valve for bundles of cylinders that convey compressed, liquefied or dissolved gases.
These are requirements for VIPRs that are in addition to those given in the relevant closure standard, for example, in ISO 10297 for cylinder valves, in ISO 17871 for quick-release cylinder valves, in ISO 17879 for self-closing cylinder valves or in ISO 23826 for ball valves. For ISO 17871, these requirements are only applicable to quick-release cylinder valves types B, C, D and E.
NOTE 1        If the pressure regulating system of a VIPR is acting as the primary valve operating mechanism, it is covered by the relevant closure standard, e.g. ISO 10297, ISO 17871, ISO 17879 and ISO 23826. This also includes designs where closure of the primary valve operating mechanism of a VIPR is obtained by closing the seat of the pressure regulating system.
NOTE 2        If the primary valve operating mechanism of a VIPR is located at the low-pressure side of the pressure regulating system, it is covered by the relevant closure standard, e.g. ISO 10297, ISO 17871, ISO 17879 and ISO 23826.
NOTE 3        The term “pressure receptacle” is used within this document to cover instances where no differentiation is necessary between gas cylinders, bundles of cylinders, pressure drums and tubes.
This document does not apply to VIPRs for
a)       medical applications (see ISO 10524-3);
b)       liquefied petroleum gas (LPG);
c)        cryogenic applications.
NOTE 4        Additional requirements for a VIPR with a residual pressure device (RPD) are specified in ISO 15996.
NOTE 5        Additional requirements for pressure relief valves can exist in international/regional regulations/ standards.

  • Draft
    39 pages
    English language
    sale 10% off
    e-Library read for
    1 day