EN 556-1:2001/AC:2006
(Corrigendum)Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devices
Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devices
TC - Modification to 4.1 and Bibliography
Sterilisation von Medizinprodukten - Anforderungen an Medizinprodukte, die als 'STERIL' gekennzeichnet werden - Teil 1: Anforderungen an Medizinprodukte, die in der Endpackung sterilisiert wurden
Stérilisation des dispositifs médicaux - Exigences relatives aux dispositifs médicaux en vue d'obtenir l'étiquetage STERILE - Partie 1: Exigences relatives aux dispositifs médicaux stérilisés au stade terminal
Sterilizacija medicinskih pripomočkov – Zahteve za medicinske pripomočke, ki morajo biti označeni s "STERILNO" – 1. del: Zahteve za končno sterilizirane medicinske pripomočke
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Frequently Asked Questions
EN 556-1:2001/AC:2006 is a corrigendum published by the European Committee for Standardization (CEN). Its full title is "Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devices". This standard covers: TC - Modification to 4.1 and Bibliography
TC - Modification to 4.1 and Bibliography
EN 556-1:2001/AC:2006 is classified under the following ICS (International Classification for Standards) categories: 11.080.01 - Sterilization and disinfection in general. The ICS classification helps identify the subject area and facilitates finding related standards.
EN 556-1:2001/AC:2006 has the following relationships with other standards: It is inter standard links to EN 556-1:2024, EN 556-1:2001. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 556-1:2001/AC:2006 is associated with the following European legislation: EU Directives/Regulations: 90/385/EEC, 93/42/EEC, 98/79/EC; Standardization Mandates: M/BC/CEN/89/9. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.
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Standards Content (Sample)
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devicesULOL]LUDQHStérilisation des dispositifs médicaux - Exigences relatives aux dispositifs médicaux en vue d'obtenir l'étiquetage STERILE - Partie 1: Exigences relatives aux dispositifs médicaux stérilisés au stade terminalSterilisation von Medizinprodukten - Anforderungen an Medizinprodukte, die als 'STERIL' gekennzeichnet werden - Teil 1: Anforderungen an Medizinprodukte, die in der Endpackung sterilisiert wurdenTa slovenski standard je istoveten z:EN 556-1:2001/AC:2006SIST EN 556-1:2002/AC:2006en,de11.080.01Sterilizacija in dezinfekcija na splošnoSterilization and disinfection in generalICS:SLOVENSKI
STANDARDSIST EN 556-1:2002/AC:200601-december-2006
EUROPEAN STANDARDNORME EUROPÉENNEEUROPÄISCHE NORMEN 556-1:2001/ACSeptember 2006Septembre 2006September 2006ICS 11.080.01English versionVersion FrançaiseDeutsche FassungSterilization of medical devices - Requirements for medical devices to bedesignated 'STERILE' - Part 1: Requirements for terminally sterilizedmedical devicesStérilisation des dispositifs médicaux -Exigences relatives aux dispositifsmédicaux en vue d'obtenir l'étiquetageSTERILE - Partie 1: Exigences relativesaux dispositifs médicaux stérilisés au stadeterminalSterilisation von Medizinprodukten -Anforderungen an Medizinprodukte, die als'STERIL' gekennzeichnet werden - Teil 1:Anforderungen an Medizinprodukte, die inder Endpackung sterilisiert wurdenThis corrigendum becomes effective on 20 September 2006 for incorporation in the three officiallanguage versions of the EN.Ce corrigendum prendra effet le 20 septembre 2006 pour incorporation dans le
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The article discusses a modification made to section 4.1 and the Bibliography of the EN 556-1:2001/AC:2006 standard. This standard pertains to the sterilization of medical devices and outlines the requirements for devices to be considered 'STERILE'. The modification to section 4.1 and the Bibliography is not further elaborated upon.
기사 제목: EN 556-1:2001/AC:2006 - 의료기기의 살균 - 'STERILE'로 지정되어야 하는 의료기기에 대한 요구사항 - 파트 1: 최종 살균된 의료기기에 대한 요구사항 기사 내용: TC - 4.1 및 참고문헌 수정 이 기사는 EN 556-1:2001/AC:2006 표준의 4.1 섹션과 참고문헌에 대한 수정 사항에 대해 논의하고 있습니다. 이 표준은 의료기기의 살균에 관련되며, 'STERILE'로 간주되기 위한 기기에 대한 요구사항을 개요로 설명합니다. 4.1 섹션과 참고문헌에 대한 수정 내용은 자세히 설명되지 않았습니다.
記事のタイトル：EN 556-1:2001/AC:2006 - 医療機器の滅菌 - 「STERILE」と指定されるための医療機器の要件 - 第1部：末期滅菌された医療機器の要件 記事内容：TC - 4.1および参考文献の修正 この記事では、EN 556-1:2001/AC:2006規格の4.1セクションと参考文献の修正について議論されています。この規格は、医療機器の滅菌に関するものであり、『STERILE』と見なされるための医療機器の要件を概説しています。4.1セクションと参考文献の修正内容については詳細には説明されていません。
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