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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Aesculap Miethke Shunt System Neurological Devices Aesculap, Inc. 2 United States USFDA
Device Recall Celsite Implantable Access Port System General Hospital and Personal Use Devices B. Braun Interventional Systems 2 United States USFDA
Device Recall B. Braun AM Aesculap Orthopedic Devices Aesculap, Inc. 2 United States USFDA
Device Recall DS Titanium Ligation Clip General and Plastic Surgery Devices Aesculap Implant Systems LLC 2 United States USFDA
Device Recall DS Titanium Ligation Clip Appliers General and Plastic Surgery Devices Aesculap Implant Systems LLC 2 United States USFDA
Prevision®-Modular Revision Prosthesis Aesculap Germany BAM
ceramic Biolox cup Aesculap Germany BAM
Metha Hip Endoprothesis Aesculap Germany BAM
Tibia Offset Stem of the ENDURO / COLUMBUS REVISION Knee System Aesculap Germany BAM
spine implant CeSpace PEEK Aesculap Germany BAM
Hydrolift spine implants AESCULAP Germany BAM
EnduRo meniscal component Aesculap Germany BAM
Plasmacup® DC polyethylene liners Aesculap Germany BAM
all Vega Tibia Extension stems Aesculap Germany BAM
the EnduRo Knee-System Aesculap Germany BAM
the Targon PF Nail AESCULAP Germany BAM
the T-Space PEEK Facelift Implants AESCULAP Germany BAM
Targon FN plate and the Telescrews AESCULAP Germany BAM
Aesculap cementless Bicontact N stem size 9 Aesculap AG Germany BAM
Columbus gliding surface/tibial insert of the article NN340 and NN222 Aesculap AG Germany BAM
Bicontact Revision Stem Aesculap AG Germany BAM
the Metha Modular Short Hip Endoprosthesis Aesculap AG Germany BAM
the Columbus Revision knee endoprosthesis Aesculap AG Germany BAM
Aesculap Plasmafit PE-Inserts Aesculap AG Germany BAM
S4 Dynamic Rod AESCULAP AG Germany BAM