Introduction To Kavo Proxam Icam - KaVo ProXam iCam Instructions For Use Manual

1 Introduction to KaVo ProXam iCam

Instructions for use
This manual describes how to set up and use the KaVo ProXam iCam
intraoral camera.
The intraoral camera KaVo ProXam iCam is meant to be used together
with Romexis or KaVo software (CONNECTbase, CONEXIO or TWAIN
Interface). It can be used in dental practices as a tool for diagnosis,
treatment planning and patient motivation.
The intraoral camera KaVo ProXam iCam can either be connected to a
KaVo treatment unit or used as a standalone version.
The intraoral camera KaVo ProXam iCam is a medical device, and the user
must be familiar with its operation. Read this manual carefully before using
the equipment.
The KaVo ProXam iCam intraoral camera unit fulfils the requirements of
Directives of (EU) 2017/745 (CE-MDR) and 2015/863/EU (RoHS).
NOTE
If the intraoral camera KaVo ProXam iCam is used together with Romexis,
Romexis software version 5.2.0.R or later is required.
NOTE
If the intraoral camera KaVo ProXam iCam is used together with a KaVo
treatment unit, ensure that the intraoral camera is connected to the treatment
unit before you switch on the treatment unit.
NOTE
The device fulfills the requirements of IEC 60601-1-2. Radio sending
equipment, like mobile phones, shall not be used in close conjunction with
the device, this can affect the device functions.
NOTE
Handle the intraoral camera according to the instructions given in this
manual. The limited warranty does not cover damage which is due to
misuse, e.g. dropping the instrument, neglect, or any cause other than
ordinary application.
NOTE
Special care must be taken when using equipment creating high
disturbances, like diathermy, so that for instance diathermy cables are not
laid upon or near the device.
NOTE
In doubtful situations contact equipment responsible person or supplier.
NOTE
External equipment intended for connection to signal input, signal output
or other connectors, shall comply with relevant IEC standard (e.g. IEC
IEC 60950-1 or IEC 62368-1 for IT equipment or IEC 60601-1 for medical
electrical equipment). In addition, all such combinations - systems - shall
comply with the standard IEC 60601-1-1, Safety requirements for medical
electrical systems. Equipment not complying to IEC 60601 shall be kept
outside the patient area, as defined in the standard.
1 Introduction to KaVo ProXam iCam
KaVo ProXam iCam 1