This device is intended for use only by persons who
have been trained in the proper interpretation of its
readings and in the appropriate safety procedures
to be followed in the presence of radiation.
These detectors are not designed, nor are they
recommended for use in primary calibration.
WARNING
CAUTION
1.1 Introduction
The VeriDose Detectors, Models 30-471 through 30-475 and 30-471-8000 through 30-475-8000, are ntype diodes utilizing a p-n junction and are designed for use as radiation detection devices. These diodes
are encased within a FDA approved polystyrene material. A low noise coaxial cable is used to connect
the diode to an electrometer. In this configuration, these diodes provide enhanced sensitivity,
instantaneous response time and are very rugged. With advantages such as large signal and fast
response, these diodes are ideal for relative measurements in areas of steep dose gradients and relative
absorbed dose in electron beam fields.
The Solid State Radiation Detector Diodes are constructed using a "parallel plate" geometry with planar
electrodes opposing each other at a given spacing. This configuration has many advantages over the
commonly used coaxial cylindrical geometry which have the electrodes being inner and outer shells.
The most obvious advantage is its superior construction and ease of orientation to the radiation beam.
Unlike the cylindrical style diodes where the alignment of the diode's sensitive volume is critical in
relationship to the radiation beam, the sensitive volume of the VeriDose Diode is the entire diode, which
allows for a less stringent alignment to the radiation beam. The hemispherical shape also allows for
easier attachment to the patient. The ideal orientation of the diode within the radiation beam is to have the
beam perpendicular to the diode's horizontal axis. As long as the beam is wider than the diode, full
collection of all ionization produced will occur regardless of the exact position in the active region.
However, for ease of alignment within a radiation
beam a raised X has been placed on top of the diode.
The VeriDose diode detectors are part of a dose monitoring system. In order to obtain accurate results,
the detectors must be used with a suitable patient dose-monitoring device. The VeriDose V, available
from Fluke Biomedical, Radiation Management Services is a 5-channel dose monitor designed
specifically for use with this type of detector. A calibration fixture is available to hold the detectors in a
fixed, reproducible geometry during the calibration process. For optimum performance, the detector must
be used within the energy range for which it was designed. Since the detectors are designed with an
internal build-up cap, additional build-up is not required.
It is recommended that the system be calibrated under clinical conditions at which the detectors will be
normally used. Since the calibration process will associate a particular detector to a specific channel on
the dose-monitoring device, it is necessary to exercise caution when reconnecting the detectors for
subsequent measurements. Each detector must be connected to the channel to which it was calibrated.
1-2
General Information
Calibration Technique
The detectors must be positioned in close proximity to the isocenter using the optional calibration fixture
or an alternative method to obtain a uniform dose. A typical exposure of 100-200 cGy at a dose rate of
100-300 cGy/min is adequate for calibration. Refer to the calibration section of the appropriate operator’s
manual for the dose-monitoring device for a complete description of the adjustment procedure. Upon
completion of the calibration process, several additional exposures should be made in the normal
measurement mode of the dose monitor in order to verify the calibration.
1
1.5 Receiving Inspection
Upon receipt of the diodes:
1. Inspect the carton(s) and contents for damage. If damage is evident, file a claim with the carrier and
contact Fluke Biomedical, Radiation Management Services at 440.248.9300.
2. Remove the contents from the packing material and visually inspect the unit for damage.
3. Verify that all items on the packing list have been received and are in good condition.
1.6 Storage
If the diodes are to be stored prior to use, pack them in the original container, if possible, and store in an
environment free of corrosive materials, fluctuations in temperature and humidity, and vibration and
shock.
1.7 Routine Cleaning
The VeriDose diodes should be kept clean and free from dirt and contamination. The unit may be
cleaned by wiping with a damp cloth, using any commercially available cleaning or decontaminating
agent.
1.8 Procedures, Warnings, and Cautions
The equipment described in this manual is intended to be used for the detection and measurement of
ionizing radiation. It should be used only by persons who have been trained in the proper interpretation of
its readings and the appropriate safety procedures to be followed in the presence of radiation.
Although the equipment described in this manual is designed and manufactured in compliance with all
applicable safety standards, certain hazards are inherent in the use of electronic and radiometric
equipment.
WARNINGS and CAUTIONS are presented throughout this document to alert the user to potentially
hazardous situations. A WARNING is a precautionary message preceding an operation which has the
potential to cause personal injury or death. A CAUTION is a precautionary message preceding an
operation which has the potential to cause permanent damage to the equipment and/or loss of data.
Failure to comply with WARNINGS and CAUTIONS is at the user's own risk and is sufficient cause to
terminate the warranty agreement between Fluke Biomedical and the customer.
Adequate warnings are included in this manual and on the product itself to cover hazards that may be
encountered in normal use and servicing of this equipment. No other procedures are warranted by Fluke
Biomedical. It shall be the owner's or user's responsibility to see to it that the procedures described here
are meticulously followed, and especially that WARNINGS and CAUTIONS are heeded. Failure on the
part of the owner or user in any way to follow the prescribed procedures shall absolve Fluke Biomedical
and its agents from any resulting liability.
1-3
Nuclear Associates 30-471
Operators Manual
Indicated battery and other operational tests must be performed prior to each use to assure that the
instrument is functioning properly. If applicable, failure to conduct periodic performance tests in
accordance with ANSI N323-l978 (R1983) Radiation Detection Instrumentation Test and Calibration,
paragraphs 4.6 and 5.4. and to keep records thereof in accordance with paragraph 4.5 of the same
standard, could result in erroneous readings or potential danger. ANSI N323-1978 becomes, by this
reference, a part of this operating procedure.
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