Revidiran
Applies to laser equipment for medical application, classified as a class 3B or class 4 laser product according to IEC 825. It deals with the particular requirements for the safety of this type of equipment including identification, marking, accuracy of operating data, protection against hazardous output and constructional requirements.
POVUČEN
IEC 60601-2-22:1992 ED1
99.60
Povlačenje stupilo na snagu
8. 11. 1995.
POVUČEN
IEC 60601-2-22:1995 ED2