BEUDAMED
    96 results · 66ms · Sources: EU EUDAMED, US FDA

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    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040234·Headed Screw Partially Threaded Short 3.0mm,32m...

    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040845·Headed Screw, Partially Threaded, Short, Diamet...

    Headed Screw Partially Threaded Short 3.0mm,30mm Length

    FDA UDI
    Pace Surgical, Inc.·00810211040227·Headed Screw Partially Threaded Short 3.0mm,30m...

    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040814·Headed Screw, Partially Threaded, Short, 5.5mm,...

    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040821·Headed Screw, Partially Threaded, Short, 6.5mm,...

    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040852·Headed Screw, Partially Threaded, Short, 6.5mm,...

    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040838·Headed Screw, Partially Threaded, Short, 6.5mm,...

    TPW 2X24IN 2-0 D/A SH,SKS-3 BWY

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code LDF·February 25, 2022

    FLEXION PACING LEAD

    FDA Adverse Event
    Malfunction ·OSCOR INC.·Product code DTB·May 6, 2024

    TPW 24IN 2-0 D/A SH,SKS-3 BWY

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code LDF·July 8, 2021

    Disposable Surgical Cable, Product Code: FL-601-97 (100), Single use, Rx Only, Remington Medical, Inc., 6830 Meadowridge Court, Alpharetta, GA 30005 Usage: Temporary pacing of open hearts: used with External Pacing Generators (EPGs).

    FDA Recall
    Terminated ·Remington Medical Inc.·Product code DSA·May 19, 2010

    TPW 24IN 2-0 D/A RB-1,SKS BWY

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code LDF·August 22, 2024

    TEMPORARY PACING LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code LDF·October 13, 2023

    ENDOWRIST

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·March 16, 2026

    ENDOWRIST

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·March 16, 2026

    ENDOWRIST

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·December 20, 2024

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·August 15, 2024

    ZY PERMANENT PACING LEAD

    FDA Adverse Event
    Injury ·OSCOR INC.·Product code DTB·September 12, 2019

    EZ STEER¿ NAV BI-DIRECTIONAL ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·January 17, 2019

    RIATA ACTIVE-FIXATION LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 29, 2006