Product group Non-active implants - bone surgery
Reference 12190/24

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

Urgent Field Safety Notice for VITELENE PE-INSERT ID 22,2, 28, 32 und 36 MM by Aesculap AG , Download_VeroeffentlichtAm_EN 2024.04.19 PDF, 3MB, File does not meet accessibility standards