Do you have a question about the Devicor Neoprobe neo2000 and is the answer not in the manual?
Brand | Devicor |
---|---|
Model | Neoprobe neo2000 |
Category | Measuring Instruments |
Language | English |
Describes the designated purpose of the device for detecting gamma radiation.
Lists medical applications for detecting radioactive emissions from body tissues or organs.
Explains the visual information and controls displayed on the LED screen.
Steps for connecting the power cord and powering on the console.
Details how the system operates and indicates radioactivity levels in Dynamic Pitch Mode.
Establishes a baseline for radioactivity levels in Dynamic Pitch Mode.
Step-by-step guide to obtaining a background count reading.
Procedure for setting the dynamic pitch range based on expected count rates.
Procedure for scanning target areas to identify radioactivity locations.
Process for identifying the intensity of gamma radiation in a specific area.
Method for calculating and displaying the ratio of target to background counts.
Procedure for obtaining a ten-second count for gamma radiation measurement.
Instructions for utilizing the autorange function to set measurement ranges.
Explains how the system indicates radioactivity above background in Binary Pitch Mode.
Establishes baseline data for radioactivity in Binary Pitch Mode.
Steps to acquire a background count in Binary Pitch Mode.
Locating radioactive areas to define target tissue boundaries in Binary Pitch Mode.
Procedure for obtaining a 6-second count of target tissue radioactivity.
Quick procedure to check radioactivity levels over target tissue.
Defines the terms and symbols used throughout the manual.
Provides detailed explanations for technical terms and graphical symbols.
Examples of using the device for external physiological and anatomical information gathering.
Use of the probe to define lymphatic flow and locate lymph nodes.
Application for localizing parathyroid adenomas during surgery.
Use in assessing bowel viability and perfusion during surgical procedures.
Assessing blood flow to anastomotic ends during surgery.
Locating small, benign bone lesions during surgery.
Safety guidelines for cleaning and disinfecting the device.
Lists approved agents for cleaning and sterilization of system components.
Steps for cleaning contamination from radioactive materials.
Detailed instructions for cleaning and disinfecting the console unit.
Detailed instructions for cleaning and disinfecting the power cord.
Procedure for replacing the console fuses.
Steps to perform system diagnostics and test visual indicators.
Procedure to test the functionality of system controls.
Procedure to verify the stability and consistency of system performance.
Steps for performing a pre-use check of the system's performance.
Table to identify and correct common operational problems.
Information regarding product service, warranty, and return policies.
Details of the warranty coverage for new products.
Technical parameters of the Model 2300 console.
Details on displayed parameters and software functionalities.
Description of the system's hardware controls and interconnects.
Safety requirements related to electrical shock, flammability, and fluid ingress.
Compliance with standards regarding electromagnetic energy emitted by the system.
Compliance with standards regarding the system's susceptibility to electromagnetic disturbances.
Guidance on maintaining immunity levels in various electromagnetic environments.
Guidelines for safe separation distances from RF transmitters.
Statement of compliance with essential requirements and provisions.
List of authorized probes and their corresponding cables.
List of approved collimators and other accessories.
Information regarding potential injuries and electrical safety precautions.
Warnings about using the device in the presence of flammable substances.