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  • Dispositivo 960
  • Fabricante 297
  • Evento 124969
  • Implante 79
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Aesculap Arcadius Trial Insertion Instrument (ME020R/ME020RUS) Orthopedic Devices Aesculap, Inc. 1 United States USFDA
Device Recall S4C Occiput Torque Wrench F/Set Screw Orthopedic Devices Aesculap, Inc. 1 United States USFDA
Device Recall Aesculap S4 Cervical (S4C) Revision Instruments (FW099R and FW101R) Orthopedic Devices Aesculap Implant Systems LLC 1 United States USFDA
Device Recall Aesculap SIBD 4 degree Trial Implant (SJ768TUS) and Aesculap SIBD 9 degree Trial Implant (SJ780TUS Orthopedic Devices Aesculap Implant Systems LLC 1 United States USFDA
Device Recall Columbus 4IN1 Femoral Cutting Guide M3 Instrument Orthopedic Devices Aesculap, Inc. 1 United States USFDA
Device Recall UNITRAC Pneumatic Retraction Arm General and Plastic Surgery Devices Aesculap, Inc. 1 United States USFDA
Device Recall Aesculap HiLine XXS handpiece General and Plastic Surgery Devices Aesculap, Inc. 1 United States USFDA
Device Recall Various B. Braun pain control convenience trays Anesthesiology Devices B. Braun Medical, Inc. 1 United States USFDA
Device Recall ASpace SIBD and Arcadius XP L systems General and Plastic Surgery Devices Aesculap, Inc. 1 United States USFDA
Device Recall Valve XS Atrium Retractable General and Plastic Surgery Devices Aesculap, Inc. 1 United States USFDA
Device Recall ASpace SIBD and Arcadius XP L systems General and Plastic Surgery Devices Aesculap, Inc. 1 United States USFDA
Device Recall B Braun Aesculap Tray Set General and Plastic Surgery Devices Aesculap, Inc. 1 United States USFDA
Device Recall Custom Spinal Anesthesia Tray General and Plastic Surgery Devices B. Braun Medical, Inc. 1 United States USFDA
GP161R; ELAN 4 1-RING DIAMOND BURR COARSE D2.0; || GP162R; ELAN 4 1-RING DIAMOND BURR+ COARSE D2.0; || GP163R; ELAN 4 1-RING DIAMOND BURR COARSE D2,3; || GP164R; ELAN 4 1-RING DIAMOND BURR+ COARSE D2,3; || GP165R; ELAN 4 1-RING DIAMOND BURR COARSE D3,0; || GP166R; ELAN 4 1-RING DIAMOND BURR+ COARSE D3,0; || GP167R; ELAN 4 1-RING DIAMOND BURR++ COARSE D3,0; || GP168R; ELAN 4 1-RING DIAMOND BURR COARSE D4,0; || GP169R; ELAN 4 1-RING DIAMOND BURR COARSE D5,0; || GP170R; ELAN 4 1-RING DIAMOND BURR COARSE D6,0; || GP173R; ELAN 4 1-RING DIAMOND BURR X-COARSE D3,0; || GP174R; ELAN 4 1-RING DIAMOND BURR X-COARSE D4,0; || GP175R; ELAN 4 1-RING DIAMOND BURR X-COARSE D5,0; || GP176R; ELAN 4 1-RING DIAMOND BURR X-COARSE D6,0; || GP177R; ELAN 4 1-RING DIAMOND BURR X-COARSE D7,0; || GP328R; ELAN 4 2-RING DIAMOND BURR X-COARSE D4.0; || GP329R; ELAN 4 2-RING DIAMOND BURR X-COARSE D5.0; || GP330R; ELAN 4 2-RING DIAMOND BURR X-COARSE D6.0; General and Plastic Surgery Devices Aesculap Implant Systems LLC 3773 Corporate Pkwy Center Valley PA 18034-8217 1 United States USFDA
GP321R; ELAN 4 2-RING DIAMOND BURR COARSE D2.3; || GP322R; ELAN 4 2-RING DIAMOND BURR COARSE D3.0; || GP323R; ELAN 4 2-RING DIAMOND BURR COARSE D4.0; || GP324R; ELAN 4 2-RING DIAMOND BURR COARSE D5.0; || GP325R; ELAN 4 2-RING DIAMOND BURR COARSE D6.0; General and Plastic Surgery Devices Aesculap Implant Systems LLC 3773 Corporate Pkwy Center Valley PA 18034-8217 1 United States USFDA
GE426R; HI-LINE XS DIAMOND BURR X-CRS.I D4.5MM; || GE426SU; HI-LINE XS DISP.DIAM.BURR X-CRS.I D4.5MM; || GE526R; HI-LINE XS DIAMOND BURR X-CRS.II D4.5MM; || GE526SU; HI-LINE XS DISP.DIAM.BURR X-CRS.II D4.5; || GE626R; HI-LINE XS DIAMOND BURR X-CRS.III D4.5MM; || GE626SU; HI-LINE XS DISP.DIAM.BURR X-CRS.III D4.5; General and Plastic Surgery Devices Aesculap Implant Systems LLC 3773 Corporate Pkwy Center Valley PA 18034-8217 1 United States USFDA
Device Recall DoyenCollin Mouth Gag 120MM/ General Instruments Ear, Nose, and Throat Devices Aesculap Implant Systems LLC 1 United States USFDA
Device Recall Strauss Penis Clamp 130MM/General Instruments Gastroenterology-Urology Devices Aesculap Implant Systems LLC 1 United States USFDA
Orthopedic Template Orthopedic Devices Aesculap Implant Systems LLC 1 United States USFDA
Device Recall Pain Control Trays Anesthesiology Devices B. Braun Medical, Inc. 2 United States USFDA
Device Recall Perifix Continuous Epidural Anesthesia Tray General Hospital and Personal Use Devices B. Braun Medical, Inc. 2 United States USFDA
Device Recall Sterile IV Start Kit General and Plastic Surgery Devices B. Braun Medical, Inc. 2 United States USFDA
Device Recall GN200 Caiman HF generators General and Plastic Surgery Devices Aesculap Implant Systems LLC 2 United States USFDA
Device Recall AESCULAP (FH620R) MINOP InVent 30 Trocar System Neurological Devices Aesculap Implant Systems LLC 2 United States USFDA
Device Recall Perifix Single Dose Epidural Anesthesia Tray General Hospital and Personal Use Devices B. Braun Medical, Inc. 2 United States USFDA
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Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.

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