Devices

Device Recall Philips Allura Xper FD10

Model / Serial
783
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
US: WA OUS: China, Spain, Korea, Republic of, Germany
Product Description
Allura Xper FD10 722026 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electro Physiology(EP).
Manufacturer
Philips Electronics North America Corporation
1 Event
- Recall of Device Recall Philips Allura Xper FD10

Manufacturer

Philips Electronics North America Corporation

Manufacturer Address
Philips Electronics North America Corporation, 3000 Minuteman Rd, Andover MA 01810-1032
Manufacturer Parent Company (2017)
Philips
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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