International Medical Devices Database

Manufacturer Address
Integra Burlington MA, Inc., 22 Terry Ave, Burlington MA 01803-2516
Manufacturer Parent Company (2017)
Integra LifeSciences Holdings Corporation
Source
USFDA
1 Event
- Recall of Device Recall Integra Life Sciences Ojemann Cortical Stimulator

One device in the database

Device Recall Integra Life Sciences Ojemann Cortical Stimulator

Model / Serial
Serial Number Range: 1010 through 1380
Product Classification
Neurological Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution-USA (nationwide) and the countries of Austria, Belgium, Czech Republic, Belgium, Denmark, Spain, Great Britain, Hungary, Ireland, Italy, Netherlands, Poland, Morocco, Netherlands, Poland, Portugal, Saudia Arabia, Sweden, Turkey, and South Africa.
Product Description
Integra Ojemann Cortical Stimulator; Product / Catalogue No: OCS2. || Intended for intraoperative cortical stimulation mapping procedures.

One manufacturer with a similar name

Learn more about the data here

Integra Burlington MA, Inc.

Manufacturer Parent Company (2017)
Integra LifeSciences Holdings Corporation
Source
DMA

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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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