Devices

Device Recall PIIC iX Intellivue iX Information Center Software

Model / Serial
All PIIC iX Surveillance stations including: 866023 IntelliVue Info Center iX A.0 866117 PIIC Classic Upgrade 866389 IntelliVue Info Center iX B.0, C.0 867141 IntelliVue Info Center iX B.0 866025 IntelliVue Server IX A.0 866118 Database Server Upgrade A.0
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Domestic and Foreign
Product Description
Intellivue iX Information Center Software - All PIIC iX Surveillance stations including: || 866023 IntelliVue Info Center iX A.0 || 866117 PIIC Classic Upgrade || 866389 IntelliVue Info Center iX B.0, C.0 || 867141 IntelliVue Info Center iX B.0 || 866025 IntelliVue Server IX A.0 || 866118 Database Server Upgrade A.0
Manufacturer
Philips Electronics North America Corporation
1 Event
- Recall of Device Recall PIIC iX Intellivue iX Information Center Software

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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