Planmeca Viso, User Manual

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19 Technical specifications
Classification
Medical Device Directive
93/42/EEC (Class IIb)
RoHS 2011/65/EU
IEC 60601‐1 Class I, type B
CISPR 11 Class B
IP Classification IPX0
Applied parts (according to IEC 60601‐1: 2012)
Patient supports
As shown in section Patient supports in User's
manuals
Patient handles
Generator (according to IEC 60601‐2‐7: 1998)
Resonant-mode, DSP-controlled, 80 ‐ 160 kHz
X‐ray tube
D-059SBR or SXR 130-10‐0.5 SC
Focal spot size (according to IEC 60336: 2005)
0.5 x 0.5 mm
Filtration
3D
Total 2.5 mm Al + 0.2 mm / 0.5 mm Cu
Pan (SmartPan) / ProCeph Total 2.5 mm Al
Tube housing front cover quality equivalent
filtration (not included in the specified total
filtration)
0.3 mm Al @ 70 kV / HVL 2.6 mm Al
Anode voltage
3D
80 ‐ 120 kV ±5%
Pan (SmartPan) 60 ‐ 84 kV ±5%
ProCeph 60 ‐ 84 kV ±5%
Anode current
3D
D-059SBR: 1‐12.5 mA ±10%
SXR 130‐10‐0.5 SC: 1‐16 mA ±10%
Pan (SmartPan) D-059SBR: 1‐14 mA ±10%
SXR 130‐10‐0.5 SC: 1‐16 mA ±10%
ProCeph D-059SBR: 14 mA ±10%
SXR 130-10‐0.5 SC: 16 mA ±10%
mAs range
min. / max. as indicated ±(10% + 0.2 mAs)
Dose range and accuracy
Dose range min. / max. as indicated on system
user interface.
Accuracy of dosimetric indication (DAP, CTDI):
±35%
Linearity of radiation output
19 Technical specifications
User's manual Planmeca Viso 103