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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Targon PF bone nails Aesculap Germany BAM
the e.motion and Columbus Femural Components Aesculap Germany BAM
Excia hip endoprothesis Aesculap Germany BAM
Bicontact S Plasmapore 12/14 size 17 mm Aesculap Germany BAM
E.motion components Aesculap AG Germany BAM
Coroflex Blue Coronarstent-systems B. Braun Germany BAM
Celsite ST301 OTW, Celsite Implantofix and Celsite Brachial B Braun Medical Sweden SMPA
celsitu injection port B. Braun Medical SAS Sweden SMPA
celsitu ST205H B Braun Medical SA Sweden SMPA
Targon United Telecommunications Screw Aesculap AG Sweden SMPA
B.Braun Celsite General Hospital and Personal Use Devices B. Braun Interventional Systems 2 United States USFDA
Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System Neurological Devices Aesculap, Inc. 2 United States USFDA
Safil QUI UNDY 5/0 (1) 45CM DSMP13 General and Plastic Surgery Devices Aesculap Implant Systems LLC 2 United States USFDA
Device Recall Metha(R) Hip System Cobalt Chrome (CoCr) Metha Modular Neck Adapters used with the Metha Modular Sho Orthopedic Devices Aesculap Inc 2 United States USFDA
Device Recall Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Orthopedic Devices Aesculap Implant Systems 2 United States USFDA
Device Recall Quintex Cervical Plating System Screws Orthopedic Devices Aesculap Implant Systems 2 United States USFDA
Device Recall Aesculap S4 Element 4.5mm Polyaxial Screws Orthopedic Devices Aesculap Implant Systems LLC 2 United States USFDA
Device Recall Aesculap(R) Miethke Shunt System Neurological Devices Aesculap, Inc. 2 United States USFDA
Device Recall Aesculap PEEK Intervertebral Body Fusion System Orthopedic Devices Aesculap, Inc. 2 United States USFDA
Device Recall Aesculap Neurological Devices Aesculap, Inc. 2 United States USFDA
Device Recall Dafilon Suture General and Plastic Surgery Devices Aesculap, Inc. 2 United States USFDA
Device Recall Aesculap Miethke Shunt System, miniNAV Valve Neurological Devices Aesculap, Inc. 2 United States USFDA
Special Materials Artificial Knee Joint Aesculap AG South Korea KFDA
Device Recall Celsite Access Port General Hospital and Personal Use Devices B. Braun Interventional Systems 2 United States USFDA
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5F7 Orthopedic Devices Aesculap, Inc. 2 United States USFDA