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REGULATORY REQUIREMENTS
International Electrotechnical Commission (IEC), international standards organization, when
applicable.
This product conforms with the Medical Device Directive, Council Directive 93/42/EEC: June 14,
1993, as amended by 2007/47/EC following the provisions of Annex II, when it bears the
following CE Mark of Conformity.
European Representative:
GE Medical Systems S.C.S.
Quality Assurance Manager
283 rue de la Minière
78530 BUC France
Tel: +33 1 30 70 40 40
Summary of Contents for Brivo OEC 715
Page 9: ...Chapter1 Introduction and Safety...
Page 34: ...Chapter2 System Overview...
Page 36: ...Brivo OEC 715 785 865 Mobile C Arm X Ray Product Page 2 3 2 2 C Arm Components...
Page 38: ...Brivo OEC 715 785 865 Mobile C Arm X Ray Product Page 2 5 2 3 Workstation Components...
Page 40: ...Chapter3 Mechanical Positioning...
Page 52: ...Chapter4 Start Up and Operating Control...
Page 77: ...Chapter5 Usual Operations...
Page 108: ...Chapter6 SpecialApplications...
Page 139: ...Chapter7 Radiographic Film...
Page 142: ...Chapter8 System Setup...
Page 149: ...System Setup Page 8 8 Click any mouse button to return to normal screen...
Page 150: ...Chapter9 Maintenance...
Page 160: ...Chapter10 Display Messages...
Page 162: ...Chapter11 Labels and Symbols...
Page 177: ...Labels and Symbols Page 11 16 42 12 15 29 40 15 13 10 18 39 31 27 24 23 37 38...
Page 179: ...Chapter12 Technical Reference...
Page 183: ...Brivo OEC 715 785 865 Mobile C Arm X Ray Product Page 12 5 Workstation Weight 170 10kg...
Page 206: ...Technical Reference Page 12 28 12 11 System Block...
Page 209: ......