Devices

Allura Xper, Allura Clarity & Integris

Model / Serial
Allura Xper, Allura Clarity & IntegrisMultiple Product names affectedAllura System product codes 722001, 722002, 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722015, 722019, 722020, 722022, 722023, 722025, 722026, 722027, 722028, 722029, 722031, 722033, 722034, 722035, 722038, 722039, 722058, 722400.Integris product codes72238, 72239, 72240, 72241, 72242, 72243 ,72244, 72245, 72246, 72247, 72248, 72249, 722021, 722030, 722043, 722044ARTG # 175708, 98560
Product Classification
Radiology Devices
Manufacturer
Philips Electronics Australia Ltd
1 Event
- Recall of Allura Xper, Allura Clarity & Integris

Manufacturer

Philips Electronics Australia Ltd

Manufacturer Parent Company (2017)
Philips
Source
DHTGA

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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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