International Medical Devices Database

Manufacturer Address
EBI, L.P., 100 Interpace Parkway, Parsippany NJ 07054-1079
Source
USFDA
1 Event
- Recall of Device Recall EBI

One device in the database

Device Recall EBI

Model / Serial
Catalog Number: S002 Lot/Serial Nos: F10021, F10017, F10012, F10018, F10025, F10019, F10020, F10014, F10023, F10022, F10001, F10000, F10024, F10007, F10008, F00005, F10003, F10016, F10015, F10002, F10027.
Product Classification
Neurological Devices
Device Class
2
Implanted device?
No
Distribution
Hospitals, clinics, and doctors nationwide.
Product Description
EBI VueCath Endoscopic Spinal System

One manufacturer with a similar name

Learn more about the data here

EBI, L.P.

Manufacturer Address
EBI, L.P., 100 Interpace Pkwy, Parsippany NJ 07054-1149
Source
USFDA

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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