Devices

Device Recall GE Centricity PACSIW Software

Model / Serial
Software version 3.7.3
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- United States (California, Illinois, Indiana, Minnesota, Nevada, New York and Wisconsin), Austria, Canada, Finland, France, Germany, Ireland, Lebanon, Japan, Philippines, Saudi Arabia, Singapore, Switzerland, Turkey, United Arab Emirates and the United Kingdom
Product Description
GE Centricity PACS-IW software; GE Healthcare Integrated IT Solutions, Barrington, IL 60010. || Device that receives, stores and communicates medical images and data from various imaging sources.
Manufacturer
Ge Healthcare It
1 Event
- Recall of Device Recall GE Centricity PACSIW Software

Manufacturer

Ge Healthcare It

Manufacturer Address
Ge Healthcare It, 540 W Northwest Hwy, Barrington IL 60010-3051
Manufacturer Parent Company (2017)
General Electric Company
Source
USFDA

One device with a similar name

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Device Recall GE Centricity PACSIW Software

Model / Serial
Software version 3.x
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide distribution: USA and Australia, Austria, Belgium, Canada, Finland, France, Germany, Hungary, India, Ireland, Israel, Italy, Japan, Korean, Kuwait, Latvia, Lebanon, Libya, Lithuania, Malaysia, Netherlands, Philippines, Poland, Qatar, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Switzerland, Turkey, United Arab Emirates and United Kingdom.
Product Description
GE Centricity PACS-IW software; GE Healthcare Integrated IT Solutions, Barrington, IL 60010. || The intended use:The Centricity PACS-IW is used to receive medical images (including mammograms) and data from various imaging sources. Images and data can be stored, communicated, processed and displayed within the system or across computer networks at distributed locations.
Manufacturer
Ge Healthcare It

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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