Philips M2268A Instrucciones De Uso página 6

Explanation of Product Symbols
These symbols can appear on the product and its associated equipment and packaging.
Symbols
Prescription use only
Storage temperature
range
Indicates the country
and date of manufacture
Medical Device
Indicates the location of
the UDI (Unique Device
Identification). Identifier
symbol with the GTIN
(Global Trade Item
Number).
It is unsafe to use the
device in MR
environments (may be
printed black on device)
Incident Reporting
Any serious incident that has occurred in relation to this device should be reported to Philips and the competent
authority of the member state in which the user and/or patient is established.
In this context "member state" refers to European Economic Area (EEA) countries including Switzerland and Turkey.
End of Life and Disposal
Visually inspect the lead sets and trunk cables for exposed wires, cracks, damaged insulation, worn connectors and
bent pins. Do not use the lead sets and trunk cables and dispose of them according to local laws for hospital waste, if
they show any of these signs.
Refer to instructions for
use
Storage pressure range
Indicates that IfU is
available in electronic
form at
www.philips.com/IFU
www.philips.com/IFU
Defibrillation-proof, type
CF applied part
Indicates the
manufacturer's catalog
number
Legal manufacturer and
address
Storage humidity range
number of pieces in
packaging
The EEG trunk cables and
lead sets comply with the
requirements of Regulation
(EU) 2017/745 of 5 April
2017 (Medical Device
Regulation).
Indicates the manufacturer's
batch code