Regulations; Symbols - Satelec Acteon P5 Newtron Manuel D'utilisation

XI - REGULATIONS
This medical device is classified as class IIa
according to European Directive relevant to
Medical Devices currently in force.
This equipment is manufactured in compliance
with the current IEC 60601-1 standard.
This equipment has been designed and
manufactured according to an ISO 13485-certified
quality assurance system.
XII - SYMBOLS
Alternating current
Class II device
BF device
Warning, please refer to the
accompanying documentation
Not to be disposed of as household
waste
CE Marking
19