XII - REGULATIONS
This medical device is classified as class IIa
according to European Directive 93/42/EEC.
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.
XIV - SYMBOLS
Alternating current
BF device
Warning, please refer to the
accompanying documentation
Not to be disposed of as household
waste
CE Marking
Irrigation
20