NF EN ISO 11990-2
Lasers and laser-related equipment - Determination of laser resistance of tracheal tubes - Part 2 : tracheal tube cuffs
ISO 11990?2:2010 specifies a method of testing the continuous wave (cw) resistance of the cuff regions of tracheal tubes designed to resist ignition by a laser. Other components of the system, such as the inflation system and shaft are outside the scope of ISO 11990?2:2010.
ISO 11990?2:2010 specifies a method of testing the continuous wave (cw) resistance of the cuff regions of tracheal tubes designed to resist ignition by a laser. Other components of the system, such as the inflation system and shaft are outside the scope of ISO 11990?2:2010.
ISO 11990?2:2010 specifies a method of testing the continuous wave (cw) resistance of the cuff regions of tracheal tubes designed to resist ignition by a laser. Other components of the system, such as the inflation system and shaft are outside the scope of ISO 11990?2:2010.
This document specifies a method of testing the continuous wave (cw) laser resistance of the shaft of a tracheal tube and the cuff regions including the inflation system of tracheal tubes designed to resist ignition by a laser. NOTE 1 When interpreting these results, the attention of the user is drawn to the fact that the direct applicability of the results of this test method to the clinical situation has not been fully established. NOTE 2 The attention of the users of products tested by this method is drawn to the fact that the laser will be wavelength sensitive and tested at the wavelength for which it is intended to be used. If tested using other wavelengths, explicitly state the power settings and modes of delivery. CAUTION ? This test method can involve hazardous materials, operations and equipment. This document provides advice on minimizing some of the risks associated with its use but does not purport to address all such risks. It is the responsibility of the user of this document to establish appropriate safety and health practices and to determine the applicability of regulatory limitations prior to use.
- Avant-propos
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1 Domaine d'application
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2 Références normatives
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3 Termes et définitions
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4 Principe
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5 Portée et utilisation de l'essai
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6 Appareillage
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7 Réactifs et matériaux
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8 Préparation des échantillons d'essai
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9 Préparation de l'appareillage
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10 Mode opératoire d'essai
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11 Interprétation des résultats
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12 Rapport d'essai
- Annexe ZA(informative) Relation entre la présente Norme européenne et les exigences essentielles de la Directive UE 93/42/CEE sur les dispositifs médicaux
- Bibliographie
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