Product group Medical electronics / Electromedical devices - electrotherapy
Reference 10696/16

For further information as well as details concerning the device please see the enclosed Advisory Notice of the manufacturer.

Recall of GN200 Lektrafuse HF Generator Bipolar, Aesculap AG , Download_VeroeffentlichtAm_EN 2017.01.20 PDF, 490KB, File does not meet accessibility standards