Devices

Device Recall B. Braun AM Aesculap

Model / Serial
All codes
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
US Nationwide Distribution
Product Description
Columbus Revision Knee System, EnduRo Knee System || Product Usage: || The Columbus Revision Knee System and EnduRo Knee System are indicated for use in reconstruction of the diseased knee joint.
Manufacturer
Aesculap, Inc.
1 Event
- Recall of Device Recall B. Braun AM Aesculap

Manufacturer

Aesculap, Inc.

Manufacturer Address
Aesculap, Inc., 3773 Corporate Pkwy, Center Valley PA 18034-8217
Manufacturer Parent Company (2017)
Ludwig G. Braun Gmbh U. Co. Kg
Source
USFDA

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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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