■X
Medical Electrical Equipment, Part 2: Particular Requirements for Safety - 37 Ultrasonic Medical
Diagnostic and Monitoring Equipment [IEC60601-2-37: 2001 with A1:2004, A2:2005]
■X
Medical Devices – Application of Risk Management to Medical Devices [ISO 14971:2007]
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Medical Electrical Equipment, Part 1: General Requirements for Safety [UL60601-1:2003]
■X
Medical Electrical Equipment, Part 1: General Requirements for Safety [CAN/CSA 22.2
No.601.1-M90:1990, with R2003, with R2005]
■X
Biological Evaluation of Medical Devices [ISO10993 : 2009]
■X
Standard Means for the Reporting of the Acoustic Output of Medical Diagnostic Ultrasonic
Equipment [IEC61157:2007]
■■
Declarations:
This is CSA symbol for Canada and United States of America.
This is manufacturer’s declaration of product compliance with applicable
EEC directive(s) and the European notified body.
This is manufacturer’s declaration of product compliance with applicable
EEC directive(s).
Commentaires sur ces manuels