Konica Minolta CS-7 Workstation with AeroDR B-1 & Battery Charger radiography system

Konica Minolta CS-7 Workstation with AeroDR B-1 and Battery Charger radiography system

Used radiography workstation and AeroDR accessory bundle comprising an HP desktop computer, EIZO monitor, keyboard and mouse, together with an AeroDR B-1 module and AeroDR Battery Charger2 cradle.

Purpose and features

The CS-7 console is used in Konica Minolta digital radiography workflows for examination management and image acquisition/processing when connected to compatible imaging equipment. 

• Installed console software: CS-7, version V1.30R02_007.
• Console serial shown in system information: A4C2-23036.
• HP desktop workstation with EIZO display, keyboard and mouse.
• AeroDR B-1 module, serial A20K-50469.
• AeroDR Battery Charger2, serial A5TJ-50248; label rating 100–240 V AC, 50/60 Hz, 180 VA.

Included

• 1 × HP computer with the photographed CS-7 software.
• 1 × EIZO monitor.
• 1 × keyboard and 1 × mouse.
• 1 × AeroDR B-1 module.
• 1 × AeroDR Battery Charger2 cradle.
  

Condition and testing

Used equipment with visible cosmetic wear;

please inspect the photographs.

DISCLAIMER: All medical items are sold in good clean and functioning condition unless otherwise stated. It is the buyers responsibility to have the item professionally tested, calibrated or serviced before clinical use on humans or animals.

NOTE: Regardless of the origin of the equipment, documentation provided or identification appearing upon the equipment, the equipment described and offered here is in no way certified for, recommended for, or offered for any specific use. The purchaser agrees that the seller shall not be held responsible or liable for any injuries or damages, whether incidental or consequential, associated in any way with the equipment. The purchaser, by offering on this equipment, indicates their acknowledgment of, and agreement to the terms of this disclaimer.

CE MARKED - This product is in compliance with the essential requirements of Council Directive 93/42/EEC Medical Device Directive, as amended by Council Directive 2007/47/EC, class IIa

NOTE: The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, we will verify your status as an authorized purchaser of this item before shipping of the item.