CEI EN 60601-1/A1 PDF

The IEC 60601 series does not apply to: 

in vitro diagnostic equipment that does not fall within the definition of ME EQUIPMENT, which is covered by the IEC 61010 series [61];

implantable parts of active implantable medical devices covered by the ISO 14708 series [69]; or 

medical gas pipeline systems covered by ISO 7396-1 [68].

NOTE 2 ISO 7396-1 applies the requirement of IEC 60601-1-8 to certain monitoring and ALARM SIGNALS.

(*) N.d.R.: Per l'elenco delle Pubblicazioni si veda l'Allegato ZA.