Devices

Device Recall OmniDiagnost

Model / Serial
OmniDiagnost User Interface PN 9896 000 59561, 9896 000 12381, 9896 000 58161; The firm utilizes a ''site number'' specific to each unit: 101599, 103055, 103058, 100520, 100873, 101152, 101154, 101676, 101962, 102164, 102582, 102977, 103050, 103051, 103052, 103055, 103058, 103218, 103219, 104012, 104577, 104858, 104934, 105324, 105394, 13124, 38351, 50428, 76596, 76944, 76948, 82655, 83871, 83958, 84441, 84850, 85163, 85165, 86113, 86303, 86326, 86339, 86340, 86485, 86486, 86549, 86965, 86977, 87164, X1707, X1747, 104857
Product Classification
Radiology Devices
Distribution
The firm distributed devices to 81 hospitals and medical centers located throughout the U.S.
Product Description
OmniDiagnost System
Manufacturer
Philips Medical Systems Sales & Service Region No. America
1 Event
- Recall of Device Recall OmniDiagnost

Manufacturer

Philips Medical Systems Sales & Service Region No. America

Manufacturer Address
Philips Medical Systems Sales & Service Region No. America, 22100 Bothell Everett Highway, Bothell WA 98041
Source
USFDA

One device with a similar name

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Device Recall OmniDiagnost

Model / Serial
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution
Product Description
OmniDiagnost
Manufacturer
Philips Medical Systems North America Co. Phillips

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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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