International Medical Devices Database

Manufacturer Parent Company (2017)
Penumbra, Inc.
Source
NIDFSINVIMA
1 Event
- Safety Alert for Penumbra System

One device in the database

Penumbra System

Model / Serial
3D, lots C00644, C00645, C00646, C00717.
Product Classification
Neurological Devices
Product Description
For use in the revascularization of patients with acute ischemic stroke.

10 manufacturers with a similar name

Learn more about the data here

Penumbra Inc.

Manufacturer Address
Penumbra Inc., 1 Penumbra, Alameda CA 94502-7610
Manufacturer Parent Company (2017)
Penumbra, Inc.
Source
USFDA

Penumbra Inc.

Manufacturer Parent Company (2017)
Penumbra, Inc.
Source
BAM

PENUMBRA Inc.

Manufacturer Parent Company (2017)
Penumbra, Inc.
Source
BAM

Penumbra Inc.

Manufacturer Parent Company (2017)
Penumbra, Inc.
Source
DH

Penumbra Inc.

Manufacturer Parent Company (2017)
Penumbra, Inc.
Source
VNSAWH

5 more

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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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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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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