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New & Used Rad/Fluoro Room, Image Intensifier

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Manf. Year From : 2001

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Please Note: Search results for this device do not include the following devices, please select the relevant device if it is of interest to you: C-Arm,Rad/Fluoro Room, Flat Panel,Cath Lab
 
 
 
 
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Device: Rad/Fluoro Room, Image Intensifier
Manufacturer: Philips
Model: Juno
Location: United States, New Jersey
Negotiable
2011

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Device: Rad/Fluoro Room, Image Intensifier
Manufacturer: Philips
Model: EasyDiagnost Eleva
Location: France, Île-de-France
20,161
This Seller accepts SafeTrade as a payment method
2004

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Device: Rad/Fluoro Room, Image Intensifier
Manufacturer: GE Healthcare
Model: Prestige II
Location: France, Île-de-France
56,702
This Seller accepts SafeTrade as a payment method
2005

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Device: Rad/Fluoro Room, Image Intensifier
Manufacturer: GMM - General Medical Merate
Model: OPERA T20C
Location: France, Provence-Alpes-Côte-d'Azur
Rating: 100%
39,061
2001

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Device: Rad/Fluoro Room, Image Intensifier
Manufacturer: Siemens
Model: SIREGRAPH TOP 40
Location: Turkey, Istanbul
19,987
2004

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Device: Cath Lab
Manufacturer: Philips
Model: MultiDiagnost Eleva
Location: United States, New Jersey
Negotiable
2004

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Device: Rad/Fluoro Room, Image Intensifier
Manufacturer: Siemens
Model: AXIOM Luminos RF
Location: France, Île-de-France
1,638
2009

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Device: Rad/Fluoro Room, Image Intensifier
Manufacturer: Philips
Model: MultiDiagnost Eleva
Location: Poland, Mazowieckie
31,501
This Seller accepts SafeTrade as a payment method
2007
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The model & manufacturer of the marked items have changed due to an acquisition between companies, and are also known as:
Current Manufacturer / Model Name Alternative Manufacturer / Model Name
GE Healthcare / Prestige II Esaote / Prestige II

Rad/Fluoro Room, Image Intensifier may also be referred to as :

Non Digital R/F Equipment | Radiographic/Fluoroscopic Table System, Image Intensifier
 

Tips for buying Rad/Fluoro Room, Image Intensifier

  1. Storage space reduction, enhanced image processing, and off-site diagnostic capabilities are some of the advantages of digital radiography over film-based radiography. Image intensifiers increase the intensity of available light in an optical system to allow use under low light conditions such as at night, to facilitate visual imaging of low-light processes such as fluorescence of materials to x-rays or gamma rays, or for conversion of non-visible light sources such as near-infrared or short wave infrared to visible.
  2. The tilting tables allow a wide range of tilting movements from -15° to +90° and have an average speed of 6°/sec. Horizontal-to-vertical tilt should average 15 sec.
  3. The non-tilting tables specify a wide range of tabletop motions but do not allow tilting angles.
  4. Digital radiographic systems generally perform upright examinations or table-based examinations, for which detector mounting is crucial.
  5. The detector is fixed in the table system in table-based units, preventing certain examinations due to patient positioning constraints. Some upright systems can be tilted to allow table based exams.
  6. Facilities should evaluate all types of examinations being performed before deciding which type of image intensifier will better suit their needs. The number and types of procedures will influence the features selected for the system.
  7. Smaller focal-spot sizes can provide better spatial resolution on film for certain studies, and options such as tomography and table tilt can increase the image intensifier system’s overall procedural capabilities.
  8. Departments handling trauma and emergency cases may prefer elevating tables because the table height can be adjusted to facilitate patient transfer from a mobile stretcher or a wheelchair.
  9. Bucky systems for both tilting and non-tilting tables should be motorized.
  10. To ensure acceptable film darkening, a three-field AEC device is recommended. Grid ratios should be 10:1 or higher. Grids with higher ratios provide higher image quality.
  11. Buyers should look into the image intensifier system’s integration into picture archiving and communication systems (PACS) already in use in the facility.
  12. Buyers should consider generator options as well; high-frequency generators need less space and often eliminate the need for high-voltage cables.
  13. To facilitate future additions to any network, compatibility with DICOM 3.0 is a requirement for all newly purchased equipment (including storage devices).
  14. Suppliers must provide DICOM conformance statements that explain in detail which information objects, service classes, and data encodings are supported by the system. The statements should be inspected by specialists, and should share the same format and vocabulary to facilitate comparisons between suppliers.
Read more valuable tips on the Medical Equipment Buying Guide by MedWOW >>