Devices

Device Recall GN200 Caiman HF generators

Model / Serial
Serial # 1229 1897 1898 1900 1909 1911 1929 1930 1932 1934 1938 1993 1997 1998 1999 2000 2029 2030 2031 2032 2037 2038 2039 2040 2041 2042 2045 2046 2047 2048 2049 2050 2051 2052 2168
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
USA (nationwide Distribution).
Product Description
GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
Manufacturer
Aesculap Implant Systems LLC
1 Event
- Recall of Device Recall GN200 Caiman HF generators

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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