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USER MANUAL
(Instruction for Use)
SW 2.9
Safety
Version 2.9.7 dated 2020-12-23
Page 14 of 75
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3.
Medical Product Operator Regulation – MPBetreibV
(Regulation valid only for Germany; please consider the valid national regulations)
4.
European Directive 2012/19/EEC (Waste Electrical and Electronic Equipment – WEEE)
(Regulation valid for EEC countries; please consider the valid national regulations)
2.3
Restrictions of Use and Safety Precautions
Please strictly follow the notes listed below:
IMPORTANT NOTE
Device use by trained personnel only!
Only authorized and suitably trained personnel should use the microkeratome
Carriazo-Pendular. The received training is annotated and must be signed in the
Medical Apparatus Book.
The Carriazo-Pendular may only be used according to the application conditions
specified by the manufacturer.
Service by trained and authorized personnel only!
Only suitably trained and from SCHWIND eye-tech-solutions authorized
personnel may perform initial installation, modifications, and service of the
Carriazo-Pendular.
Do not open the microkeratome housing!
The housing may only be opened by
authorized service personnel
Patient and Personal Safety Notes
i
2.6.1 Patient and Personal Safety,
the
installation notes
notes regarding
operation the device
and
notes for maintenance
9 Maintenance, Function Control and Storage.
2.4
Data and Virus Protection
The notes regarding data and virus protection are contained in the User Manual of the Pendular
Monitoring Software.
2.5
Manufacturer’s Responsibility
Manufacturer is only responsible for proper operation, reliability and security of the device when:
Service personnel authorized by SCHWIND eye-tech-solutions exclusively carry out transport,
installation, initial operation, changes, service and maintenance.
The power connection in the room in which the medical device is operated complies with the
legal regulations and technical specifications of SCHWIND eye-tech-solutions concerning the
installation.