Product Manual

Regulatory requirement
This product complies with regulatory requirements of the following European
Directive 93/42/EEC concerning medical devices.
This manual is a reference for the Vscan. It applies to all sub-versions of the
software version 1 for the Vscan ultrasound system unless otherwise specified.
This manual is a reference for the Vscan gateway software. It applies to all
sub-versions of the software version 1 for the Vscan gateway software unless
otherwise specified.
Manual status:
GM092207-02
26 February 2014
Manufacturer:
GE VINGMED ULTRASOUND AS
Strandpromenaden 45
N-3191 Horten, Norway
Tel.: (+47) 3302 1100 Fax: (+47) 3302 1350