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Synapse NeuRx Handbuch Seite 4

System zur atemstimulation
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p
The Keep Dry symbol appears on all packages of devices requiring to protect the
packaging from potential damage.
L
The Don't Use If Packing Damaged symbol appears on all packages of devices
requiring to dispose of the device if the packaging has suffered damage.
i
The Accompanying Documents symbol appears on all packages of devices
indicating that instructions for use are available for additional information.
C
The Regulatory Marking of Conformity symbol indicates that the device meets
2797
Medical Device Directive 93/42/EEC. This has been certified by notified body
number 2797.
P
The European Community Representative symbol indicates the identification of
the authorized representative for the distribution of devices into the European
community.
The Type BF Applied Part symbol appears on powered equipment that connects
directly to a patient. It is an indication of the degree of protection provided against
electric shock, patient leakage current and patient auxiliary current.
The Warning symbol on powered equipment indicates physiological effects not
obvious to the user that can cause harm.
The On / Off symbol on powered equipment indicates push-button ON/OFF power
control of the device.
The Consult Accompanying Documents symbol appears on powered
equipment indicating that instructions for use must be consulted for safety.
The Ingress Protection (IP) Classification symbol appears on powered
IP
24
equipment indicating that the device is protected from splashing water.
MR Unsafe. A device that is known to pose hazards in all MR environments.
Gamma Sterilization. This simple, proven process is safe, reliable, and highly
effective at treating single-use medical devices. With the ability to penetrate
4

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