BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display

    FDA Enforcement
    Class II ·Completed·Barco N.V.·July 17, 2024

    ProPlan CMF Patient-Specific Guide, Mandible guides (3A & 3B)-Intended to guide the marking of bone and/or guide surgical instruments in mandibular and maxillofacial surgical procedures. Identification number: SD900.101

    FDA Enforcement
    Class II ·Completed·Materialise N.V.·August 9, 2023

    MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched device designed to fit the patients anatomy to transfer a patient-specific pre-operative plan to the OR. Ref: KNM-ZB02-00-01

    FDA Enforcement
    Class II ·Completed·Materialise N.V.·July 26, 2023

    POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 6F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 8F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; NAUTILUS DELTA Tip Confirmation System (Includes: Netbook with Pre-loaded Software, Patient Module, and ECG Cable) Product Usage: Is an implantable access device designed to provide repeated access to the vascular system.

    FDA Recall
    Completed ·Bard Peripheral Vascular Inc·Product code LJT·June 25, 2018

    MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched device designed to fit the patients anatomy to transfer a patient-specific pre-operative plan to the OR. Ref: KNM-ZB02-00-01

    FDA Recall
    Completed ·Materialise N.V. Technologielaan 15 Heverlee Belgium·Product code JWH·April 26, 2023

    ProPlan CMF Patient-Specific Guide, Mandible guides (3A & 3B)-Intended to guide the marking of bone and/or guide surgical instruments in mandibular and maxillofacial surgical procedures. Identification number: SD900.101

    FDA Recall
    Completed ·Materialise N.V. Technologielaan 15 Heverlee Belgium·Product code JEY·June 19, 2023

    MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display

    FDA Recall
    Completed ·Barco N.V. President Kennedypark 35 Kortrijk Belgium·Product code DXJ·April 24, 2024