Product group Non-active implants - bone surgery
Reference 01927/16

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

Batch recall for BIOLOX DELTA REVISION HEAD 12/14 32MM S, Aesculap AG , Download_VeroeffentlichtAm_EN 2016.03.21 PDF, 213KB, File does not meet accessibility standards