Optomed Aurora 7
European certificate of conformity
The CE marking with notified body identification numbering indicates the conformity
of 93/42/ EEC Medical Device Directive for class IIa devices and CE marking without
notified body identification numbering indicates the conformity of 93/42 EEC
Medical Device Directive for class I devices.
Read the instructions for use carefully
Failure to follow these instructions could place the patient or operator at risk.
Radio frequency radiation
The device has WLAN functionality. Electromagnetic interference may occur in
the vicinity of equipment.
FCC Declaration of conformity
The device emits RF radiation. Electromagnetic interference from the device is
under limits approved by the Federal Communications Commission.
Prescription device
Symbol for : “Caution: Federal law restricts this device to sale by or on the order
of a physician or licensed practitioner.”
Type BF applied parts
The eye cup which is in physical contact with the patient, is electrically isolated
and protected against electric shock.
Class II power supply
For indoor use only
Power supply designed primarily for indoor use only according to IEC 60417
Safety |
To Next Page
Loading...
