iTeh StandardsiTeh Standards
EURUSD
Your shopping cart is empty.
CEN

EN 1499:1997

(Main)

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

Chemical disinfectants and antiseptics - Hygienic handwash - 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 handwash reduces the release of transient flora according to the requirements when used for washing the artificially contaminated hands of volunteers. 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, forexample: - in hospitals, in community medical facilities and in dental institutions; - in clinics of schools, of kindergardens and of nursing homes.

Chemische Desinfektionsmittel und Antiseptika - Desinfizierende Händewaschung - 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 desinfizierende Händewaschung die Abgabe der transienten Flora entsprechend denAnforderungen verringert, wenn es für das Waschen der künstlich kontaminierten Hände von freiwilligen Probanden verwendet wird. Die Europäische Norm gilt für Produkte zur desinfizierenden Händewaschung, die in Bereichen und unter Bedingungen angewendet werden, wo eine Desinfektion medizinisch angezeigt ist.

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

La présente norme européenne décrit une méthode d'essai simulant des conditions pratiques afin d'établir si un produit pour le lavage hygiénique des mains réduit la flore transitoire conformément aux exigences lorsqu'il est utilisé pour laver les mains artificiellement contaminées de volontaires. La présente norme européenne s'applique aux produits destinés au lavage hygiénique des mains utilisés dans les zones et les situations où la désinfection est médicalement préconisée.

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

General Information

Status
Withdrawn
Publication Date
18-Mar-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 1499:2001 - Chemical disinfectants and antiseptics - Hygienic handwash - Test method and requirements (phase 2/step 2)

Relations

Replaced By
EN 1499:2013 - Chemical disinfectants and antiseptics - Hygienic handwash - Test method and requirements (phase 2/step 2)
Effective Date
08-Jun-2022

Buy Standard

EN 1499:2001EN 1499:2001
PreviousNext
Standard
EN 1499:2001
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 - Desinfizierende Händewaschung - Prüfverfahren und Anforderungen (Phase 2/Stufe 2)Antiseptiques et désinfectants chimiques - Lavage hygiénique des mains - Méthode d'essai et prescriptions (phase 2/étape 2)Chemical disinfectants and antiseptics - Hygienic handwash - 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 antiseptikiDisinfec
...

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 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 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 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 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 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 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 12625-5:2024(Main)
Tissue paper and tissue products - Part 5: Determination of wet tensile strength (ISO 12625-5:2024)
SIST EN ISO 12625-5:2024

This document specifies a test method for the determination of the wet tensile strength of tissue paper and tissue products after soaking with water, using a tensile-strength-testing apparatus operating with a constant rate of elongation.
Currently, two types of tensile-strength-testing apparatus are commercially available, one where the test piece is positioned vertically and, for the other, horizontally. This document applies for both. For vertical tensile-strength-testing apparatus, a device that is held in the lower grip of the tensile-strength-testing apparatus, called a Finch Cup, is used to achieve the wetting. For horizontal tensile-strength-testing apparatus, the soaking device is placed between the two clamps.
This document is not applicable to cases where impurities and contraries are determined.

  • Standard
    22 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    20 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
CEN ISO/TR 5601:2024(Main)
Paints and varnishes - Determination of volatile organic compound (VOC) and/or semi-volatile organic compound (SVOC) content - Best practices for the selection of test methods (ISO/TR 5601:2023)
kSIST-TP FprCEN ISO/TR 5601:2024

This document aims to enable users to identify an appropriate method for the determination of volatile organic compounds (VOC) content and/or the semi-volatile organic compounds (SVOC) content of coating materials and their raw materials. This document provides a step-by-step procedure for identifying appropriate tests. This document is intended to be used in conjunction with ISO 11890-1, ISO 11890-2 and ISO 17895, to help users select an appropriate analytical method for their analytical problem.

  • Draft
    9 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN 12662-1:2024(Main)
Liquid petroleum products - Determination of total contamination - Part 1: Middle distillates and diesel fuels
kSIST FprEN 12662-1:2024

This document specifies a method for the determination of the content of undissolved substances, referred to as total contamination, in middle distillates, in diesel fuels containing up to 30 % (V/V) fatty acid methyl esters (FAME). The working range is from 12 mg/kg to 26 mg/kg and it was established in an interlaboratory study by applying EN ISO 4259-1 [4].
This document in general is applicable to products having a kinematic viscosity not exceeding 8 mm2/s at 20 °C, or 5 mm2/s at 40 °C.
This test method can be used for paraffinic diesel fuels as specified in EN 15940, for diesel fuels containing more than 30 % (V/V) FAME and for petroleum products having a kinematic viscosity exceeding 8 mm2/s at 20 °C, or 5 mm2/s at 40 °C, however in such cases the precision of the test method has not been determined.
NOTE   For the purposes of this document, the term “% (V/V)” is used to represent the volume fraction, φ, of a material.
WARNING - The use of this document can involve hazardous materials, operations and equipment. This document does not purport to address all of the safety problems associated with its use. It is the responsibility of the user of this document to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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