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Medical Electrical Equipment - Part 2: Particular Requirements for the Safety of Transcutaneous Partial Pressure Monitoring Equipment (Adopted IEC 601-2-23:1993) / Appareils électromédicaux - Partie 2: Règles particulières de sécurité pour les appareils de surveillance de la pression partielle transcutanée (norme CEI 601-2-23:1993 adoptée)
Publication Year 1998
Published by CSA Group
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This Particular Standard specifies the particular requirements for the safety of TRANSCUTANEOUS PARTIAL PRESSURE MONITORING EQUIPMENT as defined in 2.101, hereinafter referred to as EQUIPMENT.
This Standard applies to transcutaneous monitors used with adults, children and neonates and includes the use of these devices in foetal monitoring during birth.
This Standard does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin (for example conjunctiva, mucosa). /
Domaine d'application
La présente Norme Particulière spécifie les règles particulières de sécurité des APPAREILS DE SURVEILLANCE DE LA PRESSION PARTIELLE TRANSCUTANÉE définis en 2.101, et désignés ci-après par le terme APPAREIL.
La présente Norme s'applique aux moniteurs transcutanés utilisés sur des adultes, des enfants et des nouveau-nés, et elle inclut l'utilisation de ces dispositifs dans la surveillance foetale pendant l'accouchement.
La présente Norme ne s'applique pas aux oxymètres à hémoglobine saturée ou aux dispositifs appliqués sur des surfaces du corps autres que la peau (par exemple conjonctive, muqueuse).
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