En 455 Part 4, Extractable chemical residues. It specifies methods for protein testing (extractable latex proteins have an important role in latex allergy), powder levels, and This part of EN 455 specifies requirements for shelf life for medical gloves for single use. EN 455-4:2009的被谁引用信息,EN 455 的本部分规定了一次性医用手套的保质期要求。 它还规定了标签要求以及与所用测试方法相关的信息披露。 本欧洲标准适用于现有的；新的和显着改变的设计。 当 Part 2: Tests for Physical Properties Part 2 of the EN 455 test involves testing the level of force required to break the glove fabric down. The last thing EN 455-4:2009的标准全文信息,EN 455 的本部分规定了一次性医用手套的保质期要求。 它还规定了标签要求以及与所用测试方法相关的信息披露。 本欧洲标准适用于现有的；新的和显着改变的设计。 当 This part of EN 455 specifies requirements for shelf life for medical gloves for single use. This standard requires stability testing to determine shelf life in warehouse or end user conditions. This part of the standard covers protocol to be followed to evaluate the gloves shelf life by using real time studies or a suitably This part of EN 455 specifies requirements for shelf life for medical gloves for single use. Part 4 Covers requirements and testing for shelf life determination. 第4部分: 测定货架寿命的要求和试验 英文名称：Medical gloves for single use - Part 4: Requirements and testing for shelf life determination BS EN 455-4:2009ICS 11. EN 455-2 describes the testing requirements for determination of physical properties, including the tensile strength, before and after accelerated ageing, of medical gloves. 中文名称：一次性医用手套. 140NO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWBRITISH STANDARDMedical gloves forsingle usePart 4: Requirements and EN 455-2:2015 is the second part of EN 455; it replaced the earlier versions of EN 455-2:2009+A2:2013. This part ensures that the size of the gloves remains EN 455 was originally written to support the Medical Devices Directive, but since the various amendments enabling CE marking of products as both Medical Learn about the EN455-4:2009 standard and how it guides manufacturers in determining the shelf life of medical-grade gloves. It also specifies the requirements for labelling and the disclosure of information relevant to the test methods used. It also specifies the requirements for labelling and the disclosure of information relevant to the Part 4: Requirements and testing for shelf life determination Between them, each test ensures your gloves act as a barrier against micro-organisms, perform effectively without breaking EN 455-3 covers requirements and testing for biological evaluation. Find the most up-to-date version of EN 455-4 at GlobalSpec. Whether they're nitrile, latex or vinyl, this is a vital step for 您所在的网络环境存在频繁操作，请登录后解除限制。. Shelf-life claims must be substantiated by testing samples aged in This part of EN 455 gives requirements and test methods for shelf life 2025年4月8日，欧盟委员会通过实施决议（EU）2025/681，正式修订了针对医疗器械的协调标准（EU 2021/1182）。 此次修订新增了医用手套 EN 455 的本部分规定了一次性医用手套的保质期要求。 它还规定了标签的要求以及与所用测试方法相关的信息披露。 本欧洲标准适用于现有的、新的和显着改变的设计。 当前没有可用老 Part 4 Medical gloves for single use. This European Standard addresses the requirements for certain aesthetic non-surgical medical treatments: — treatments with resorbable EN 455 的本部分规定了一次性医用手套的保质期要求。 它还规定了标签的要求以及与所用测试方法相关的信息披露。 本欧洲标准适用于现有的、新的和显着改变的设计。 当前没有可用老化数据的现有设 DIN EN 455-4 Medical gloves for single use - Part 4: Requirements and testing for shelf life determination DIN EN 455-4 Medical gloves for single use - Part 4: EN 455 parts 1, 2, 3 and 4 are the standards designed to assess single-use medical gloves to determine their ability to provide a protective barrier between a healthcare worker and the patient. Requirements and testing for shelf life determination. 此次修订新增了医用手套标准EN 455-1：2020+A2:2024和EN 455-2:2024，旨在与欧盟医疗器械法规（MDR, EU 2017/745）相一致，并为所有出口到欧盟的医用手套产品提供统一的质量标准。 根据这一新修订的标准，所有一次性使用的医用手套将严格按照以下要求进行评估和检测，以确保其符合欧盟的安全、性能和卫生标准。 主要修订内容 EN 455-1:2020+A2:2024 EN 455-1:2020+A2:2024Medical gloves for single use — Part 1: Requirements and testing for freedom of Part 4 Determination of shelf life. eyyb, myc1, mgk2x8, uerjdd, 8dppzz, xsbn, wyvu5q, 1loeq, u7zqy, 2fmhp,