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  • DUTCH, pagina 145

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Type B device
In accordance with Directive 93/42/EEC
0086
Disposal in compliance with WEEE
Consult the instructions for use
Caution: Consult the accompanying documents
Manufacturer
Date of Manufacture
Serial number
Single patient use
Federal U.S. law restricts this device to sale by or
on the order of a physician. (Rx only)
Medical Device listing mark for US and Canada by
SGS Testing Services recognised by the American
Occupational Safety and Health Administration
(OSHA) for electrical safety and compliance.
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