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XVI - 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 developed
according to an ISO 13485-certified quality
assurance system.
XVII - SYMBOLIQUE
Alternating current
BF device
Warning, please refer to the
accompanying documentation
Not to be disposed of as household
waste
CE marking
27

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