Devices

Device Recall AESCULAP (FH620R) MINOP InVent 30 Trocar System

Model / Serial
Item # FH620R
Product Classification
Neurological Devices
Device Class
2
Implanted device?
No
Distribution
Product was distributed throughout the United States and Canada.
Product Description
AESCULAP MINOP InVent 30 Trocar System, non-sterile || Product Usage:The Minop InVent Trocar System intended use is for endoscopic procedures within the central nervous system, especially for the treatment of intra- and paraventricular pathological structures.
Manufacturer
Aesculap Implant Systems LLC
1 Event
- Recall of Device Recall AESCULAP (FH620R) MINOP InVent 30 Trocar System

Manufacturer

Aesculap Implant Systems LLC

Manufacturer Address
Aesculap Implant Systems LLC, 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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