Devices

Device Recall Aesculap(R) Miethke Shunt System

Model / Serial
Lots 4503489878, 4503792749, 4503682927, 4503508385, 4503789879, 4503800248 and 4503682935.
Product Classification
Neurological Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution including MI, PA and TX.
Product Description
Aesculap(R) - Miethke Shunt System, FT040T - Control Reservoir Set w/Distal Catheter and FT075P 0 Ventric Cathet, w/Stylet and RT-ANG Guide || Central Nervous System Shunt and Components intended to shunt cerebrospinal fluid (CSF) from the lateral ventricles of the brain into the peritoneum.
Manufacturer
Aesculap, Inc.
1 Event
- Recall of Device Recall Aesculap(R) Miethke Shunt System

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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