Devices

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
Manufacturer
EBI, L.P.
1 Event
- Recall of Device Recall EBI

Manufacturer

EBI, L.P.

Manufacturer Address
EBI, L.P., 100 Interpace Parkway, Parsippany NJ 07054-1079
Source
USFDA

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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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