Devices

Device Recall Regius

Model / Serial
All serial numbers.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
These units have been distributed to hospitals and clinics nationwide.
Product Description
Regius-IM. The Regius Image Manager for Centralized workflow and improved image quality software.
Manufacturer
Konica Medical Imaging, Inc.
1 Event
- Recall of Device Recall Regius

Manufacturer

Konica Medical Imaging, Inc.

Manufacturer Address
Konica Medical Imaging, Inc., 411 Newark Pompton Tpke, Wayne NJ 07470-6657
Source
USFDA

2 devices with a similar name

Learn more about the data here

Device Recall REGIUS IM, RIM

Model / Serial
58 units distributed between June 2003 and January 2006. Software version prior to January 31, 2006.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
The units were distributed to hospitals nationwide through the firm''s sales force and resellers. There are no government accounts.
Product Description
REGIUS Image Manager (AKA REGIUS IM, RIM). Catalogue Number 5900554. Centralized CR Image Quality Control. Patient throughput optimization via offloaded processing from various CR readers. Technologist review and audit. Key processing for specialized exams, totally automated processing for hands off operation. Centralized workflow device for dispersed readers environments. HIS/RIS patient status updates. Demographic Correction.
Manufacturer
Konica Minolta Medical Imaging USA, Inc.

Device Recall Regius

Model / Serial
Serial # 0729-0005
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Texas
Product Description
Regius Model 370 Digital Radiography || Konica Minolta
Manufacturer
Konica Minolta Medical Imaging USA, Inc.

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Disclaimer

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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