SIST EN 13726-6:2003
(Main)Non-active medical devices - Test methods for primary wound dressing - Part 6: Odour control
Non-active medical devices - Test methods for primary wound dressing - Part 6: Odour control
This European Standard describes a test method for the evaluation of waterproofness of primary wound dressings when such claims are made.
Nichtaktive Medizinprodukte - Prüfverfahren für primäre Verbandstoffe (Wundauflagen) - Teil 6: Geruchsbindung
Dispositifs médicaux non-actifs - Méthodes d'essai pour les pansements primaires en contact avec la plaie - Partie 6: Contrôle de l'odeur
La présente Norme européenne décrit une méthode d'essai permettant d'évaluer la résistance a la pénétration des odeurs de pansements primaires en contact avec la plaie.
Neaktivni medicinski pripomočki – Preskusne metode za sanitetni material za primarno oskrbo rane - 6. del: Kontrola vonja
General Information
Standards Content (Sample)
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Nichtaktive Medizinprodukte - Prüfverfahren für primäre Verbandstoffe (Wundauflagen) - Teil 6: GeruchsbindungDispositifs médicaux non-actifs - Méthodes d'essai pour les pansements primaires en contact avec la plaie - Partie 6: Contrôle de l'odeurNon-active medical devices - Test methods for primary wound dressing - Part 6: Odour control11.120.20Sanitetni materiali, obveze in kompreseWound dressings and compressesICS:Ta slovenski standard je istoveten z:EN 13726-6:2003SIST EN 13726-6:2003en01-september-2003SIST EN 13726-6:2003SLOVENSKI
STANDARD
SIST EN 13726-6:2003
EUROPEAN STANDARDNORME EUROPÉENNEEUROPÄISCHE NORMEN 13726-6April 2003ICS 11.120.20English versionNon-active medical devices - Test methods for primary wounddressing - Part 6: Odour controlDispositifs médicaux non-actifs - Méthodes d'essai pour lespansements primaires en contact avec la plaie - Partie 6:Contrôle de l'odeurNichtaktive Medizinprodukte - Prüfverfahren für primäreVerbandstoffe (Wundauflagen) - Teil 6: GeruchsbindungThis European Standard was approved by CEN on 28 February 2003.CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this EuropeanStandard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such nationalstandards may be obtained on application to the Management Centre or to any CEN member.This European Standard exists in three official versions (English, French, German). A version in any other language made by translationunder the responsibility of a CEN member into its own language and notified to the Management Centre has the same status as the officialversions.CEN members are the national standards bodies of Austria, Belgium, Czech Republic, Denmark, Finland, France, Germany, Greece,Hungary, Iceland, Ireland, Italy, Luxembourg, Malta, Netherlands, Norway, Portugal, Slovakia, Spain, Sweden, Switzerland and UnitedKingdom.EUROPEAN COMMITTEE FOR STANDARDIZATIONCOMITÉ EUROPÉEN DE NORMALISATIONEUROPÄISCHES KOMITEE FÜR NORMUNGManagement Centre: rue de Stassart, 36
B-1050 Brussels© 2003 CENAll rights of exploitation in any form and by any means reservedworldwide for CEN national Members.Ref. No. EN 13726-6:2003 ESIST EN 13726-6:2003
EN 13726-6:2003 (E)2ContentspageForeword.3Introduction.41Scope.52Terms and definitions.53Test method for odour penetration.53.1Significance and use.53.2Equipment.53.3Procedure.63.4Results.73.5Test report.7SIST EN 13726-6:2003
EN 13726-6:2003 (E)3ForewordThis document (EN 13726-6:2003) has been prepared by Technical Committee CEN /TC 205, "Non-active medicaldevices", the secretariat of which is held by BSI.This European Standard shall be given the status of a national standard, either by publication of an identical text orby endorsement, at the latest by October 2003, and conflicting national standards shall be withdrawn at the latestby October 2003.EN 13726 consists of the following Parts under the general title Non-active medical devices - Test methods forprimary wound dressings:Part 1: Aspects of absorbencyPart 2: Moisture vapour transmission rate of permeable film dressingsPart 3: WaterproofnessPart 4: ConformabilityPart 5: Bacterial barrier propertiesPart 6:Odour controlAccording to the CEN/CENELEC Internal Regulations, the national standards organizations of the follo
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