BEUDAMED
    23 results · 27ms · Sources: EU EUDAMED, US FDA

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    PROBEAM PROTON THERAPY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Causse

    FDA UDI
    MEDTRONIC XOMED, INC.·00681490034579·PROSTHESIS 1133191 CAUSSE MALLEUS LOOP

    Causse

    FDA UDI
    MEDTRONIC XOMED, INC.·00763000035204·PROSTHESIS 1133191 CAUSSE MALLEUS LOOP

    Oticon

    FDA UDI
    Oticon A/S·05707131260611·RIA PRO, MINIRITE 312 WL DBL

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613024925·Metzenbaum Scissors, Super Cut, Curved, Blunt B...

    SOHNIKS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    QUADROX-I PEDIATRIC MICROPOROUS MEMBRANE OXYGENATOR WITH INTEGRATED ARTERIAL FILTER WITH SOFTLINE / BIOLINE COATING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M.U.S.T. PEDICLE SCREW 7X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017

    PEDICLE SCREW 03.50.030 PEDICLE SCREW 7X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 3, 2020

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 29, 2013

    EPIC II CRITICAL CARE BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·May 4, 2011

    KOTEX SECURITY TAMPONS - SUPER

    FDA Adverse Event
    Injury ·KIMBERLY-CLARK CORP., CONWAY MILL·Product code HEB·August 21, 2008

    MECTALIF POSTERIOR

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·October 8, 2025

    MECTALIF OBLIQUE INTERBODY FUSION DEVICE PEEK/TI 12X28X7 L0°

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code MAX·November 10, 2017

    MECTALIF (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI 11X22X7 L5

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·April 29, 2020

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X30 LONG HEAD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·May 23, 2019

    MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·May 25, 2023

    PEDICLE SCREW PEDICLE SCREW 6X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·September 21, 2018

    MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code MAX·October 17, 2018

    syngo.via RT Image Suite with syngo.via VB30, VB40, VB50 and VB60- Intended for Radiation Therapy Treatment Material Number: 10496180

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc·September 22, 2021