Safety
Instructions for use • OR1 SmartScreen • PQJ219_EN_V1.0_04-2021_IFU_CE-MDR 8
Additional devices connected to electrical medical equipment must comply with the relevant
IEC or ISO standards. Furthermore, all configurations must comply with the requirements for
medical electrical systems (see Clause 16 of IEC 60601-1).
Only combine the product with devices and components that are approved for joint use by
the manufacturer.
The product should not be used immediately adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, the product should be observed to verify normal
operation in the configuration in which it will be used.
Comply with national and local regulations.
Only make changes to the product if these changes are approved by KARLSTORZ.
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