15
ELECTROMAGNETIC COMPATIBILITY
This device was designed to meet the current requirements for electromagnetic compatibility (EN 60601-1-2). Electro-
medical devices require particular care during installation and use relative to EMC requirements. Users are therefore
requested to install and/or use these devices following the manufacturer's specifications. Potential electromagnetic in-
terference with other devices. RF mobile or portable radio and telecommunications devices (mobile telephones or wire-
less connections) might interfere with the operation of electro-medical devices. For additional information please go
to www.flaemnuova.it. The device may be subject to electromagnetic interference if other devices are used for specific
diagnosis or treatments. Flaem reserves the right to make technical and functional modifications to the product with no
prior warning.
SYMBOLS
TÜV Certification
Medical CE Marking ref. Dir. 93/42 EEC and
subsequent updates
Device serial number
Class II device
Manufacturer
Attention: check the instructions for use
Type BF applied part
Operating switch off
Alternating current
Operating switch on
Keep dry
In compliance with: European Standard EN
10993-1 ''Biological Evaluation of medical
devices'' and the European Directive 93/42/EEC
''Medical Devices''. Phthalate-free. In compli-
ance with: Reg. (EC) no. 1907/2006
Minimum and maximum atmospheric pressure
Minimum and maximum room temperature
Minimum and maximum air moisture
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