Devices

Device Recall Philips Intellispace Portal

Model / Serial
Software release 4.0.0
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- US, including states of IN and TX, and countries of Australia, Austria, Czech, Denmark, France, Germany, Indonesia, Netherlands, Poland, Spain, and Switzerland.
Product Description
Philips Intellispace Portal, Release 4.0.0. || For storing, processing and management of electronic information/data || Model: 881001. || Indicated for use as a diagnostic device.
Manufacturer
Philips Medical Systems Nederlands
1 Event
- Recall of Device Recall Philips Intellispace Portal

Manufacturer

Philips Medical Systems Nederlands

Manufacturer Address
Philips Medical Systems Nederlands, Veenpluis 4-6, Best Netherlands
Manufacturer Parent Company (2017)
Philips
Source
USFDA

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Disclaimer

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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