Devices

Philips Allura Xper Systems

Model / Serial
Model: multiple, Affected:
Manufacturer
Philips Medical Systems Nederland BV
1 Event
- Recall of Philips Allura Xper Systems

Manufacturer

Philips Medical Systems Nederland BV

Manufacturer Parent Company (2017)
Philips
Source
NZMMDSA

2 devices with a similar name

Learn more about the data here

Device Recall Philips Allura Xper Systems

Model / Serial
Velara Generator with 12nc number: 989000070011, 989000070122, 989000070123, 989000070124, 989000070125, 989000070126, 989000070321
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
US: AL, CA, DC, IL,GA, KS, MD, MO, NC, NY, OH, PA, RI, SC, TX, WA OUS: Brazil, Bulgaria, Costa Rica, France, Germany, Israel, Italy, Japan, Korea, Republic of, Mexico, Russian Federation, Singapore, Spain, Sweden, Switzerland Switzerland, Turkey, United Kingdom
Product Description
Velara Generator with an old Firmware version used with Philips Allura Xper Systems (Allura 15 & 12 (monoplane), Allura FD10C, Allura FD10F, Allura FD 10 F/C, Allura FD20, Allura XPER FD10/10, Allura XPER FD20 Biplane)
Manufacturer
Philips Electronics North America Corporation

the Philips Allura Xper systems and Allura CV20

Model / Serial
Product Description
Radiological technology
Manufacturer
Philips

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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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