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FLAEM SC36P00 Manual De Instrucciones página 17

Aparato para aerosolterapia

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  • MX

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  • MEXICANO, página 27
SYMBOLS
CE Medical Marking ref. Dir. 93/42
EEC and subsequent amendments
Class II device
Important: check the operating
instructions
"OFF" for part of equipment
"ON" for part of equipment
Complies with: European standard
EN 10993-1 "Biological Evaluation
of Medical Devices" and European
Directive 93/42/EEC "Medical Devices".
Phthalates free. In conformity with
Reg. (EC) no. 1907/2006
Minimum and maximum room
temperature
Minimum and maximum
atmospheric pressure
ELECTROMAGNETIC COMPATIBILITY
This device was designed to satisfy the currently required requisites 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. Risk of
potential electromagnetic interference with other devices. Mobile or portable RF
radio and telecommunication devices (mobile phones or wireless connections) may
interfere with the operation of medical devices. For more information, visit the website
www.flaemnuova.it. The appliance may be susceptible to electromagnetic interference
in the presence of other devices used for specific diagnoses or treatments. Flaem
reserves the right to make technical and functional changes to the product without
prior notice.
Certification TÜV
Serial number of device
Manufacturer
Type BF applied part
Alternating current
Enclosure protection rating: IP21.
IP21
(Protected against solid bodies over
12 mm. Protected against access
with a finger. Protected against
vertically falling water drops.)
Minimum and maximum air
moisture
15

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