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Normas DIN – AENOR
DIN ISO 21881:2018-08

DIN ISO 21881:2018-08

Sterile packaged ready for filling cartridges (ISO/DIS 21881:2018); Text in German and English / Note: Date of issue 2018-07-20

Conditionnement stérile des cartouches prêtes à l'emploi (ISO/DIS 21881:2018); Texte en allemand et anglais / Attention: Date de parution 2018-07-20

Sterilverpackungen für die Abfüllung vorgefertigter Kartuschen (ISO/DIS 21881:2018); Text Deutsch und Englisch / Achtung: Erscheinungsdatum 2018-07-20

Fecha Anulación:
2020-12 /Withdrawn
Equivalencias internacionales:

ISO/DIS 21881 (2018-05)

Relación con otras normas DIN:

Reemplazada por: DIN ISO 21881:2020-12

This document specifies the characteristics of sterile and ready for filling empty glass cartridges for injectable preparations, including the minimum requirements of materials, packaging systems and analytical test methods. In the last few years, following the more and more urgent request for ready for filling containers, packaging manufacturers managed to offer to the pharmaceutical industry containers already washed and sterilized. This category of products was born about thirty years ago with the appearance on the market of ready for filling syringes. Due to the increasing market presence of syringes "ready for filling" and the associated advantages of this product for the pharmaceutical industry, the suppliers of packaging materials started to develop systems of this type for cartridges. The availability of two packaging configurations makes ready for filling glass cartridges suitable to be used both in clinical trials and in mass production. Nest and tub configuration has been conceived to be used usually with automated filling machines, while tray configuration is usually suitable for small batches filled manually or by means of semi-automated filling machines.
Bottling, Bottlings, Cartridges, Characteristics, Cleaning, Closures, Definitions, Design, Disposable, Disposables, Drying, Filling, Glass, Glass containers, Glassware, Injection bottles, Injection containers, Injection instruments, Injection preparations, Injections, Materials, Means of packaging, Medical devices, Medical equipment, Medical products, Medical sciences, Medical technology, Packages, Packaging glass, Packaging material, Packaging processes, Parenteral infusion equipment, Performance requirements, Plastic containers, Prefabricated, Protection, Protective container, Quality, Quality management, Specification (approval), Sterile, Sterile barrier systems, Sterility, Sterilization (hygiene)
Idioma Formato

Formato digital

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