Devices

Device Recall DPXBravo/Duo

Model / Serial
software versions 12.0, 12.1, 12.2,13.0, & 13.1.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution
Product Description
DPX-Bravo/Duo, GE Lunar DEXA bone densitometers operating with enCORE software versions 12.0, 12.1, 12.2,13.0, & 13.1. || The systems provide an estimate of BMD.
Manufacturer
Ge Healthcare
1 Event
- Recall of Device Recall DPXBravo/Duo

Manufacturer

Ge Healthcare

Manufacturer Address
Ge Healthcare, 9900 W Innovation Dr, Wauwatosa WI 53226-4856
Manufacturer Parent Company (2017)
General Electric Company
Source
USFDA

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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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