Devices

Device Recall Diagnost 56/66/76/76 Plus

Model / Serial
Devices are identified as Site Numbers: 73421, 46653, 59224, 62325, 13479, 46954, 25563, 61812, 34800, 13612, 13624, 68220, 35590, 68219, 17576, 59474, 35420, 62630, 44890, 41239, 13691, 59011, 47149, 44888, 6709, 6824, X1007, and X1775.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution
Product Description
Diagnost 56/66/76/76 Plus, DSI is a Spot-Film and has a Digital Imaging Spot. || Intended use is for the following applications: as a multifunctional/universal system, general R/F, Fluoroscopy, Radiology, and Angiography can be performed along with pediatric examinations and more specialized interventional applications.
Manufacturer
Philips Medical Systems North America Co. Phillips
1 Event
- Recall of Device Recall Diagnost 56/66/76/76 Plus

Manufacturer

Philips Medical Systems North America Co. Phillips

Manufacturer Address
Philips Medical Systems North America Co. Phillips, 22100 Bothell Everett Hwy, Bothell WA 98021-8431
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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