Devices

Device Recall System, Endovascular Graft Aortic Aneurysm Treatment

Model / Serial
Lot Numbers: W06-0079, W06-0334, W06-0393, W06-0501, W06-0658, W06-0773, W06-0988 & W06-1196
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
Worldwide, including USA and Germany.
Product Description
Endologix Infrarenal Bifurcated Powerlink System with Visifiex Delivery System (endovascular graft), Model Number 28-16-155BL
Manufacturer
Endologix Inc
1 Event
- Recall of Device Recall System, Endovascular Graft Aortic Aneurysm Treatment

Manufacturer

Endologix Inc

Manufacturer Address
Endologix Inc, 11 Studebaker, Irvine CA 92618-2013
Source
USFDA

One device with a similar name

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Device Recall System, Endovascular Graft Aortic Aneurysm Treatment

Model / Serial
Lot Numbers: W06-0333, W06-0392, W06-0500, W06-0553, W06-0621, W06-1100 & W06-1152
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
Worldwide, including USA and Germany.
Product Description
Endologix Infrarenal Bifurcated Powerlink System with Visifiex Delivery System (endovascular graft). Model Number 25-16-155BL
Manufacturer
Endologix Inc

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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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