Note 3 to entry: The primary purpose of information supplied by the manufacturer is to identify the medical device and its manufacturer, and provide essential information about its safety, performance, and appropriate use to the user or other relevant persons. Like Taking into account the specific and additionally occurring interferences, these elements can be determined in water and digests of water and sludge (e. Resumen: This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of non-critical medical devices not intended to be sterilized (i. This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of non-critical medical devices not intended to be sterilized (i. Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014) EN ISO 11135:2014/A1:2019. Gegenüber der DIN EN ISO 17664:2004-07 [2] wurden Änderungen vorgenom - Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11. EN ISO 17664-2:2023. No. UNI EN ISO 17664:2018 Condizionamento dei prodotti per la cura della salute - Informazioni che devono essere fornite dal fabbricante del dispositivo medico per il condizionamento dei dispositivi medici La norma specifica i requisiti relativi alle informazioni che devono essere fornite dal fabbricante di dispositivi medici riguardanti Dec 20, 2023 · Adoptada de: ISO 17664-2:2021. en langue Française et au format HTML et PDF. Portuguese. a medical device that is intended to come into contact with intact skin only or a medical device not intended for direct patient contact). Die Novellierung der DIN EN ISO 17664:2017 bietet einen guten Anlass, die Veränderungen der Norm anzuschauen und auch Konsequenzen für die Praxis auf - zuzeigen. a medical device that is intended to come into contact with intact skin only or a medical device not intended ab 186,60 EUR inkl. Ausgabedatum: 2024 04. Oct 26, 2018 · Glossario. BS EN ISO 17664-2:2023 Processing of health care products. Main. EN ISO 11135:2014. EN ISO 11607-2:2020 Opakowania dla finalnie sterylizowanych wyrobów medycznych – Część 2: Wymagania dotyczące walidacji procesów formowania, uszczelniania i montowania (ISO 11607-2:2019) EN ISO 11607-2:2020/A1:2023 25. Sep 1, 2023 · Draft Document - Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021); German and English version prEN ISO 17664-2:2023. 10. EVS-EN 50360:2017. FR Recognition Number. Note 4 to entry: See Figure 1. ISO 17664-2:2021 Traitement de produits de soins de santé — Informations relatives au traitement des dispositifs médicaux à fournir par le fabricant du dispositif Partie 2: Dispositifs médicaux non critiques DIN EN ISO 17664-2:2024-04 (D) Aufbereitung von Produkten für die Gesundheitsfürsorge - Vom Medizinprodukt-Hersteller bereitzustellende Informationen für die Aufbereitung von Medizinprodukten - Teil 2: Unkritische Medizinprodukte (ISO 17664-2:2021); Deutsche Fassung EN ISO 17664-2:2023 Inhalt Seite This document excludes processing of: 1) critical and semi-critical medical devices; 2) medical devices intended to be sterilized; 3) textile medical devices used in patient draping systems or surgical clothing; 4) medical devices specified by the manufacturer for single use only and supplied ready for use. Pages. Give feedback. Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021); German and English version prEN ISO 17664-2:2023 . Jan 10, 2024 · Manufacturers,Medical equipment,Information,Products,Health care services Jan 7, 2024 · EUROPEAN STANDARD NORME EUROPÉENNE EUROPÄISCHE NORM EN ISO 17664-2 December 2023 ICS 11. Mar 24, 2023 · Die ISO 17664-2 beinhaltet Informationen zur wirksamen Aufbereitung der nicht-kritischen Produkte ohne Sterilisation. 2023-08-09. NOTE See ISO 17664-2:2021, AnnexE, for NF EN ISO 17664-1. 01 Sterilization and disinfection in general> BS EN ISO 17664-2:2023 Processing of health care products. Each member body interested in a subject for which a technical ISO 17664-2:2021(E) Foreword ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). Apr 30, 2024 · Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021) May 30, 2022 · FR Recognition List Number. 16. This product standard applies to wireless communication devices used in close proximity to the human ear (e. Mar 8, 2024 · Packaging for terminally sterilized medical devices – Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019) EN ISO 11607-2:2020/A1:2023. : ISO 17664-2. Voir plus. 4. ABNT NBR ISO 17664-2 - 2023-08-09 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices Part 2: Non-critical medical device. 25. CHF 105,00 DIN EN ISO 17664-2. Voir moins. It also provides methods to substantiate the use of 25 kGy or 15 kGy as the sterilization dose to achieve a sterility Jan 10, 2024 · ISO 17664-2. 00 En ligne En ligne ISO 17664-2:2021(E) Foreword ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). Scope. 2015. a medical device that enters normally sterile parts of the human body or a medical device that comes into contact with mucous membranes or non-intact skin) or medical devices that are intended to be sterilized. Date of Entry 05/30/2022. Zurück zum Seitenanfang. 12. Erfahren Sie mehr über den Normen-Ticker. 01 English Version Processing of ealth care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021) Traitement de produits de soins santé - Informations relatives au traitement des Jul 6, 2021 · Rather, this document specifies requirements to assist manufacturers of medical devices in providing detailed processing instructions that consist of the following activities, where applicable: j) transportation. Source: CEN. EN ISO 17664-2:2023 Processing of health care products – Information to be provided by the medical device Publication date. It contains additional requirements specific to organizations involved in the life cycle of medical devices, while other elements of ISO 9001 have been removed that are not relevant as regulatory requirements. This is the first edition of CSA ISO 17664-2:2023, Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non- critical medical devices , which is an adoption without modification of the identically titled ISO (International Organization for Standardization) Standard ISO 17664-2 (first May 9, 2024 · 该文档贡献者很忙,什么也没留下。 This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of non-critical medical devices not intended to be sterilized (i. 2023. Information to be provided by the medical device manufacturer for the processing of medical devices Non-critical medical devices While ISO 13485 is a stand-alone standard, it is similar in scope and intent to ISO 9001, Quality management systems. Alle 26 anzeigen. 080. Processing of health care products – Information to be provided by the medical device manufacturer for the processing of medical devices May 2, 2023 · Amendment. a medical device that is intended to come into contact with intact ab 215,10 EUR inkl. EVS-EN ISO 11137-2:2015. Norme En vigueur. standard by DIN-adopted European-adopted ISO Standard, 09/01/2023. B. International Standards that specify requirements for validation and routine control of sterilization processes require when it is necessary to supply a sterile medical device, that adventitious microbiological contamination of a medical device prior to sterilization be minimized. DIN EN ISO 17664-1 - 2021-11 Aufbereitung von Produkten für die Gesundheitsfürsorge - Vom Medizinprodukt-Hersteller bereitzustellende Informationen für die Aufbereitung von Medizinprodukten - Teil 1: Kritische und semi-kritische Medizinprodukte (ISO 17664-1:2021); Deutsche Wegweisend für ein sachgerechtes Vorgehen bei der Reinigung von Medizinprodukten sind neben § 4 MPBetreibV und den diesbezüglichen mandatierten europäischen Normen (z. Normes remplacées (1) NF ISO 17664-2. org/directives). 07/15/2019: Sterility: 14-531: Complete: ISO : 11607-2 Second edition 2019-02 1) critical and semi-critical medical devices; 2) medical devices intended to be sterilized; 3) textile medical devices used in patient draping systems or surgical clothing; 4) medical devices specified by the manufacturer for single use only and supplied ready for use. 35. This document excludes processing of: 1) critical and semi-critical medical devices; 2) medical devices intended to be sterilized; 3) textile medical devices used in patient draping systems or surgical clothing; 4) medical devices specified by the manufacturer for single use only and supplied ready for use. septembre 2021. Relación con otras normas BSI: : ISO 17664-2:2021. May 17, 2022 · Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021) 2. Jetzt informieren! CSA Preface . En revanche, le présent document spécifie des exigences visant à aider les fabricants de dispositifs médicaux à fournir des instructions de traitement détaillées qui comprennent, le cas échéant, les activités suivantes: a) la préparation avant le traitement; b) le nettoyage; c) la désinfection; d) le séchage; e) le contrôle et la Sep 1, 2023 · Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021), German and English version prEN ISO 17664-2:2023 Sep 2, 2021 · Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices Part 2: ledna, 2022. Categories: Sterilization and disinfection. ISO 17664-1:2021の規格概要 この文書は、クリティカルまたはセミクリティカルな医療機器(すなわち、人体の通常は無菌部分に入る医療機器または粘膜と接触する医療機器)の処理のために医療機器メーカーによって提供される情報の要件を Apr 24, 2022 · 4、请认真阅读上述条款,您发帖即代表接受上述条款。. Przetwarzanie produktów do ochrony zdrowia – Informacje dostarczane przez wytwórcę wyrobu medycznego dotyczące przetwarzania wyrobów medycznych – Część 2: Wyroby medyczne niskiego ryzyka (ISO 17664-2:2021) Buy ISO 17664-2:2021 Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices Part 2: Non-critical medical devices from Intertek Inform BS EN ISO 17664-2:2023 Processing of health care products. NOTE See Annex E for further guidance on the application of the ISO 17664 A sterile medical device is one that is free of viable microorganisms. Information to be provided by the medical device manufacturer for the processing of medical devices Non-critical medical devices (British Standard) NF EN ISO 17664-2:2023 NF S98-116-2:2023 Format En ligne + PDF Vous permet d'accéder en ligne au document PDF et de le télécharger. ISO 11137-2 specifies methods for determining the minimum dose needed to achieve a specified requirement for sterility. 下载积分: 2000. 29. NOTE See Annex E for further guidance Mar 12, 2021 · ISO 17664-2-2021. DIN EN ISO 17664-2 (DRAFT) : 2023. Zusätzlich erfolgt durch diese Veröffentlichung eine Aktualisierung der Empfehlung 46 des FA Qualität. 2017. Name. ISO/IEC 17025 Allgemeine Anforderungen an die Kompetenz von Prüf- und Kalibrierlaboratorien ANSI/AAMI/ISO 17664-2:2022; Processing of health care products—Information to be provided by the medical device manufacturer for the processing of medical devices—Part 2: Non-critical medical devices CSA Preface This is the first edition of CSA ISO 17664-2:2023, Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non- critical medical devices , which is an adoption without modification of the identically titled ISO (International Organization for Standardization) Standard ISO 17664-2 (first Feb 19, 2020 · Abstract. a medical device that is intended to NF EN ISO 17664-2:2023,Traitement de produits de soins de santé - Informations relatives au traitement des dispositifs médicaux à fournir par le fabricant du dispositif - Partie 2 : dispositifs médicaux non critiques. ISO 18562-2:2017 specifies tests for the emissions of particulate matter from the gas pathways of a medical device, its parts or accessories, which are intended to provide respiratory care or supply substances via the respiratory tract to a patient in all environments. PDF 24,40 € koos KM-ga 12/18/2023: Sterility: 14-595: Complete: ISO : 11607-2 Second edition 2019-02 [Including AMD1:2023] Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes [Including Amendment 1 (2023)]. DIN EN ISO 17664 - 2018-04 Aufbereitung von Produkten für die Gesundheitsfürsorge - Vom Medizinprodukt-Hersteller bereitzustellende Informationen für die Aufbereitung von Medizinprodukten (ISO 17664:2017); Deutsche Fassung EN ISO 17664:2017. The working range depends on the matrix and the interferences encountered. Type. Apr 26, 2024 · en iso 11607-2:2020 EN ISO 17664-2:2023 Implementing Decision (EU) 2024/817 amending Implementing Decision (EU) 2021/1195 as regards harmonized standards for medical gloves for single use, biological evaluation of medical devices, sterilization of health care products, packaging for terminally sterilized medical devices and processing of health Discover new articles every week on the topics of regulatory affairs (including international approval and FDA approval), QM systems (e. 07. Original language. Non-critical medical devices. Schnelle Zustellung per Download oder Versand. DIN EN ISO 15883 sowie 17664) die Aussagen von Kommission für Krankenhaushygiene und Infektionsprävention und des BfArM in den „Anforderungen an die Hygiene bei der Mar 8, 2024 · EN ISO 11607-1:2020/A1:2023 24. 표준번호 표준명 발행일 상태; 1: DIN EN ISO 17664-2:2024-04: Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021); German version EN ISO 17664-2:2023 Aug 15, 2023 · Amendment. Sep 26, 2007 · ISO 21535:2007. Aufbereitung von Produkten für die Gesundheitsfürsorge - Vom Medizinprodukt-Hersteller bereitzustellende Informationen für die Aufbereitung von Medizinprodukten - Teil 2: Unkritische Medizinprodukte. MwSt. Traitement de produits de soins de santé - Informations relatives au traitement des dispositifs médicaux à fournir par le fabricant du dispositif - Partie 1 : dispositifs médicaux critiques et semi-critiques. Sistema : proceso para eliminar, destruir o desactivar microorganismos en superficies de productos a un nivel previamente especificado para su uso previsto. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. Information to be provided by the medical device manufacturer for the processing of medical devices. NOTE See Annex E for further guidance on the application of the ISO 17664 series to a medical device. Details of 日本規格協会のWeb販売サイト「JSA Webdesk」のページです。日本産業規格JISや国際規格ISO・IEC、海外規格ASTM・BS・DIN・ASME・UL等の規格販売。品質管理や信頼性等の管理技術、ISOマネジメントシステム、標準化、規格説明会、国際標準化研修など様々な研修メニューがございます。 2) medical devices intended to be sterilized; 3) textile medical devices used in patient draping systems or surgical clothing; 4) medical devices specified by the manufacturer for single use only and supplied ready for use. iso. The goal of the validation is to ensure that the identified process is able to properly process the medical device to make it suitable to be used for its intended use. 14-578. EVS-EN ISO 17664-2:2023. Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices. Norme Annulée. ISO 17664-1 First edition 2021-07. : EN ISO 17664-2:2023. Inform now! E DIN EN ISO 17664-2:2023-09 (D/E) Erscheinungsdatum: 2023-08-04 Aufbereitung von Produkten für die Gesundheitsfürsorge - Vom Medizinprodukt-Hersteller bereitzustellende Informationen für die Aufbereitung von Medizinprodukten - Teil 2: Nicht kritische Medizinprodukte (ISO 17664-2:2021); Deutsche und Englische Fassung prEN ISO 17664-2:2023 Oct 5, 2021 · ISO PDF プレビュー. 11. EN ISO 17664-2:2023 Przetwarzanie produktów do ochrony zdrowia – Informacje dostar L'ISO 17664 :2017 spécifie les exigences relatives aux informations devant être fournies par un fabricant de dispositifs médicaux concernant le traitement d'un dispositif médical qui nécessite un nettoyage, puis une désinfection et/ou une stérilisation afin de s'assurer qu'il est sûr et efficace pour son utilisation prévue. Medizinprodukte (ISO 17664-2:2021) This European Standard was approved by CEN on 17 December 2023. This document specifies requirements for hip-joint replacement implants. ČSN EN ISO 17664-1 připravuje se. 058. g. This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of critical or semi-critical medical devices (i. EN ISO 11607-2:2020 Packaging for terminally sterilized medical devices – Part 2: Vali dation requirements for forming, sealing and assembly processes (ISO 11607-2:2019) EN ISO 11607-2:2020/A1:2023 25. 080 Sterilization and disinfection>11. 内容提示: Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices —Part 2: Non-critical medical devicesTraitement de produits de soins de santé — Informations relatives au traitement des dispositifs médicaux à Oct 5, 2021 · Next > ISO 8351-2:1994 包装—袋の仕様方法—パート2. 回帖后跳转到最后一页. In den Warenkorb. Sie hilft mit einem Flowchart bei der Zuordnung, ob ein Produkt unter den Anwendungsbereich der ISO 17664-1 oder den der ISO 17664-2 fällt. View all product L’identification de ces types de clauses repose sur le document « Directives ISO/IEC, Partie 2 - Principes et règles de structure et de rédaction des documents ISO » ainsi que sur une liste de formes verbales constamment enrichie. EN ISO 11137-1:2015 Série EN / AS 9100 système d'assurance de la qualité pour le marché aéronautique et spatial VDA Qualitäts Management Center SAE J1939 - Vehicle bus recommended practice Oct 5, 2021 · ISO 17664-2:2021の規格概要 この文書は、滅菌することを意図していない重要でない医療機器(すなわち、無傷の皮膚のみと接触することを意図した医療機器またはそうでない医療機器)の処理のために医療機器メーカーによって提供される情報の要件を指定します直接の患者との接触を目的として May 3, 2021 · Estas definiciones se toman directamente de ISO 17664. 求ISO 17664-1和17664-2 2021版,求ISO 17664-1和17664-2,蒲公英 - 制药技术的传播者 GMP理论的实践者. EN ISO 17664-1:2021 - Zpracování výrobků pro zdravotní péči - Informace, které mají být poskytnuty výrobcem zdravotnických prostředků - Část 1: Kritické a semikritické zdravotnické prostředky. Avec Exigences, accédez rapidement à l’essentiel du texte normatif ! This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of critical or semi-critical medical devices (i. Meditsiiniseadme tootja esitatav teave meditsiiniseadmete töötlemiseks. Le présent document spécifie les exigences relatives aux informations à SS-EN ISO 17664-1:2021 Rengöring, desinfektion samt sterilisering av medicintekniska produkter - Information som ska tillhandahållas av tillverkaren för återanvändning av medicinsk tekniska produkter - Del 1 Kritiska och halvkritiska medicintekniska produkter (ISO 17664-1:2021) EVS-EN ISO 17664-2:2023 Tervishoiutoodete töötlemine. EVS-EN ISO 11137-2:2015/A1:2023. Dieses Dokument legt die Anforderungen an This document is available in either Paper or PDF format. Or download the PDF of the directive or of the official journal for free DIN EN ISO 17664-1:2021 DE Aufbereitung von Produkten für die Gesundheitsfürsorge - Vom Medizinprodukt-Hersteller bereitzustellende Informationen für die Aufbereitung von Medizinprodukten - Teil 1: Kritische und semi-kritische Medizinprodukte (ISO 17664-1:2021); Deutsche Fassung EN ISO 17664-1:2021 Manufacturers,Medical equipment,Information,Products,Health care services Dec 1, 2023 · 2) medical devices intended to be sterilized; 3) textile medical devices used in patient draping systems or surgical clothing; 4) medical devices specified by the manufacturer for single use only and supplied ready for use. Mar 8, 2024 · EN ISO 11607-1:2020/A1:2023 24. The process which is identified in the information provided along with the medical device shall be validated. e. The work of preparing International Standards is normally carried out through ISO technical committees. Scope/Abstract. digests of water as described in ISO 15587-1 or ISO 15587-2). medical devices specified by the manufacturer for single use only and supplied ready for use. EVS-EN 50360:2017/A1:2023. Committee: CH/198 - Sterilization and Associated Equipment and Processes. CHF 86. Aufbereitung von Produkten für die Gesundheitsfürsorge - Vom Medizinprodukt-Hersteller bereitzustellende Informationen für die Aufbereitung von Medizinprodukten - Teil 2: Unkritische Medizinprodukte (ISO 17664-2:2021); Deutsche Fassung EN ISO 17664-2:2023. The applicable frequency range is from 300 MHz to 6 GHz. ISO 17664-2:2021-02. Acht Praxistipps zur Umsetzung der ISO 17664. ISO shall not be held responsible for identifying any or all such patent rights. , ISO 13485), risk management (ISO 14971), software development (IEC 62304), IT security, clinical evaluation, usability engineering (IEC 62366-1), and systems engineering (including IEC 60601-1, ISO 10993 DIN EN ISO 17664-2:2024 Format Online + PDF Ermöglicht Ihnen, online auf das PDF-Dokument zuzugreifen und es herunterzuladen. Each member body interested in a subject for which a technical Standard [NEW] DIN EN ISO 17664-2:2024-04 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021); German version EN ISO 17664-2:2023 DIN EN ISO 17664-2:2024 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021); German version EN ISO 17664-2:2023 Feb 25, 2021 · This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of non-critical medical devices not intended to be sterilized (i. Limpieza : eliminación de contaminantes de un artículo en la medida necesaria para su posterior procesamiento r para el uso previsto. Requirements for Validation of the Process according to ISO 17664. CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this EN ISO 17664-2:2023 - Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices Part 2: Non-critical medical devices. editorial rules of the ISO/IEC Directives, Part 2 (see www. 02. Draft standard [WITHDRAWN] DIN EN ISO 17664-2:2023-09 - Draft Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021); German and English version prEN ISO 17664-2:2023 Dec 20, 2023 · Infórmate sobre la EN ISO 17664-2:2023 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021)¡Entra y cómprala! View the "EN ISO 17664-2:2023" standard description, purpose. août 2021. mobile phones, wireless headsets). DIN EN ISO 17664-2 - 2024-04 Aufbereitung von Produkten für die Gesundheitsfürsorge - Vom Medizinprodukt-Hersteller bereitzustellende Informationen für die Aufbereitung von Medizinprodukten - Teil 2: Unkritische Medizinprodukte (ISO 17664-2:2021); Deutsche Fassung EN ISO 17664-2:2023. ČSN. 3. ISO 17664-2:2021の規格概要 この文書は、滅菌することを意図していない重要でない医療機器(すなわち、無傷の皮膚のみと接触することを意図した医療機器またはそうでない医療機器)の処理のために医療機器 Dec 29, 2023 · Date. With regard to safety, this document specifies requirements for intended performance, design attributes, materials, design evaluation, manufacture, sterilization, packaging, information supplied by the manufacturer and methods of test. Standard. ab 201,03 EUR exkl. Customers who bought this document also bought: IEC-60529 Degrees of protection provided by enclosures (IP Code) SIS-EN-ISO-13485 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) ASTM-F1980 Standard Guide for Accelerated Aging of Mar 8, 2024 · EN ISO 11607-2:2020/A1:2023. gl vg gr pn nr kr nc hg ju ay