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Avis d'intention
Sondes d'aspiration pour les voies respiratoires...
This document specifies dimensions and requirements for both open and closed suction catheters made of flexible materials and intended for use in suctioning of the respiratory tract. Suction catheters intended for use with...
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Systèmes de gestion de l'énergie - Lignes directrices...
This document gives practical guidelines and examples for establishing, implementing, maintaining and improving an energy management system (EnMS) in accordance with the systematic approach of ISO 50001:2018. The guidance in...
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Stérilisation des produits de santé - Indicateurs...
The ISO 11138 series provides manufacturers and others with the requirements for production, labeling, test methods and performance requirements of biological indicators used to develop, validate and monitor sterilization...
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Biocarburants solides - Manipulation et stockage...
Note: The standards activity type for this NOI was updated by the responsible SDO on March 16 ,2021. ISO 20024-2020 provides principles and requirements for safe handling and storage of solid biofuels pellets in commercial...
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Cordons et câbles flexibles
1.1 General This standard specifies the requirements for flexible cords, elevator cables, and hoistway cables rated 600 V maximum and electric vehicle cables rated 1000 V maximum and intended for use in accordance with CAN...
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Outils électroportatifs à moteur, outils portables...
This clause of Part 1 is applicable, except as follows: Addition: This part of IEC 62841 applies to hand-held hammers. Tools covered by this document include percussion hammers and rotary hammers, including rotary hammers...
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Emballages des dispositifs médicaux stérilisés...
The ISO 11607-1 specifies requirements and test methods for materials, preformed sterile barrier systems, sterile barrier systems and packaging systems that are intended to maintain sterility of terminally sterilized medical...
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Emballages des dispositifs médicaux stérilisés...
The ISO 11607-2 specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing and assembly of preformed sterile...
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Stérilisation des produits de santé – Irradiation...
ISO 11137-4 provides additional guidance to that given in ISO 11137-3 on meeting the requirements specified in ISO 11137-1 , ISO 11137-2 and ISO/TS 13004 for the establishment and control of a radiation sterilization process...
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Sterilisation des produits de sante – Methodes...
The ISO 11737-2 specifies the general criteria for tests of sterility on medical devices that have been exposed to a treatment with the sterilizing agent which has been reduced relative to that anticipated to be used in...
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Dispositifs de sécurité et de commande pour brûleurs...
This document specifies safety, construction, performance and testing requirements for controls for gasburners and gas burning appliances for use with natural gas, manufactured gas or liquefied petroleum gas(LPG). This...
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Dispositifs de sécurité et de commande pour brûleurs...
This document specifies safety, constructional and performance requirements of valve-proving systems (VPS), intended for use with gas burners and gas -burning appliances. It also describes the test procedures for checking...