BEUDAMED
    23 results · 23ms · Sources: EU EUDAMED, US FDA

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    Aveta Disposable Hysteroscope

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707069591·D.B. BRACKET REMOVING PLIERS

    GALILEO® LEFTY TIGHTY™ CRT²™ LAG SCREW, LEFT, 10.5mm x 100mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665036558·

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702825305·ELVAREX 3/KNEE HIGH/SLANT-CLOSED TOE-ELEPHANTIA...

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780419020·Integra® Miltex® Micro Ear Forceps 3" Shaft, 4....

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111000·INSTRUMENT CADDY SMALL

    LEFTY TIGHTY LAG SCREW, Ø10.5MMX100MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HSB·October 16, 2024

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780419037·Integra® Miltex® Micro Ear Forceps 3" Shaft, 4....

    M2 NAVIGATION CATHETER AND GUIDELINER NAVIGATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDER-FREE, YELLOW VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DUETTO MT

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM S.P.A.·Product code GEX·April 14, 2022

    LEFTY TIGHTY LAG SCREW, Ø10.5MMX100MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HSB·October 20, 2025

    SPECTRUM IQ INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·March 2, 2023

    GALILEO LAG SCREW, RIGHT, Ø10.5MMX110MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HSB·June 8, 2024

    GALILEO LAG SCREW, RIGHT, Ø10.5MMX100MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HSB·June 8, 2024

    LEFTY TIGHTY LAG SCREW, Ø10.5MMX100MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HSB·June 7, 2024

    TROCHANTERIC NAIL, 10MM X 20CM X 130°

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HSB·June 7, 2024

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·October 7, 2008

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL NEUROMODULATION·Product code LGW·June 20, 2013

    SENSIA SR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code NVZ·August 4, 2011