Recall for the E-tegra Stent Graft System, JOTEC GmbH
2015.08.11
Product group Non-active implants - special implants
Reference 04689/15
For further information as well as details concerning the device please see the enclosed Advisory Notice of the manufacturer.
Recall for the E-tegra Stent Graft System, JOTEC GmbH , Download_VeroeffentlichtAm_EN