X-ray Tube

HOME > PRODUCTS > TUBES

  OCX/65-G  
DESCRIPTION AND TECHNICAL DATA
Voltage
nominal
70 kV
maximum for test
80 kV
Inverse voltage
nominal
85 kV
maximum for test
93 kV
Focal spot (IEC 60336:2005)
0,8 mm
Filament characteristics
4 +/- 0,1 max 2,8
Anode material
tungsten
Target angle
19 °
Anode heat storage capacity
7500 J
Maximum anode cooling rate
110 W
Maximum anode cooling rate
110 W
Inherent filtration
0,5 mm Al
Maximum diameter
30 mm
Overall length
85 mm
DIMENSIONS AND CONNECTIONS
Zoom
PATTERNS OF MAXIMUM DC
CHARACTERISTICS OF ISSUANCE AND FILAMENT
GENERAL INFORMATIONS When mounting tube inserts adopt proper caution, in order to avoid glass bulb breaking and fragments projection. Please use protective gloves and glasses. Tube insert connected to H.V. supply is a radiation source: be sure to take all necessary safety cautions
  • Wash thoroughly with alcohol the external surface of tube insert (care of fi re risk). Avoid contact of dirty surfaces with cleaned tube insert.
  • Clamp system inside housing or self-contained units must not mechanically stress the tube.
  • After installation, check the right working of the tube (no fl uctuation of tube current nor crackling)
  • Comply with insert thermal parameters, planning and programming the exposure parameters and cooling pauses. Housing or self-contained units must be provided with an adequate thermic protection.
  • Voltages indicated in charts are valid for transformer supplied with ground center.
  • It is extremely important to observe the connection diagram and the grid resistor value. Any change could modify the dimensions of the focal spot, also varying diagnostic performances or overloading anode target.
  • Tube inserts contain environment polluting materials, particularly lead liner tubes. Please apply to qualifi ed operator for waste disposal, according to local regulation requirements.
INCIDENT REPORT ACCORDING TO 93/42/EEC MEDICAL DEVICES DIRECTIVE
In order to comply with CE marking requirements, end users have to report to local Competent Authority all the informations about possible incidents involving the device, regarding any deterioration in its characteristics and performances, as well as any inaccuracies in this documentation, which might lead to or might have led to the death of patient / user or a deterioration in his state of health. This information must be promptly reported also to C.E.I. in order to start manufacturer reporting, as per above mentioned directive.
This mark assures device conformity to EC Directive 93/42 on Medical Devices Safety
PRODUCT SEARCH
duty circle
PRODUCT CATEGORIES
DENTAL
VETERINARY
INDUSTRIAL CONTROL
QUALITY CONTROL
ALIMENTARY
CONTACT U.S.
I accept the privacy policy
NEWSLETTER



Accetto l'informativa sulla privacy
 

ABOUT U.S.
IL NOSTRO PASSATO E IL NOSTRO PRESENTE 1956 L'ing. Giovanni Bottonelli fonda a Bologna...
[read more...]
Tel. (+39)  051.6285800
Fax. (+39) 051.6259245
info@cei-xray.it