Devices

Allura Xper FD20 R8.2

Model / Serial
Allura Xper FD20 R8.2System Code: 722028Serial Number: 460ARTG Number: 225815
Manufacturer
Philips Electronics Australia Ltd
1 Event
- Recall of Allura Xper FD20 R8.2

Manufacturer

Philips Electronics Australia Ltd

Manufacturer Parent Company (2017)
Philips
Source
DHTGA

One device with a similar name

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Device Recall Philips Allura Xper FD20 R8.2 722028

Model / Serial
1000
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
US: WA OUS: China, Spain, Korea, Republic of, Germany
Product Description
Allura Xper FD20 R8.2 722028 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electrophysiology(EP).
Manufacturer
Philips Electronics North America Corporation

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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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