BEUDAMED
    24 results · 21ms · Sources: EU EUDAMED, US FDA

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    CORDIS TRAPEASE PERMANENT VENA CAVA FILTER WITH THE VISEASE ANGIOGRAPHIC VESSEL DILATOR; MODELS 466-P306AU & 466-P306BU

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65820203161·OBTURATOR - OBT20 - SIZE 25 Obt 20pk CHC2

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040109912·OBTURATOR - OBT20 - SIZE 25 Obt 20pk CHC2

    Midway Select

    FDA UDI
    MIDWAY DENTAL SUPPLY, LLC·10843717103155·Midway Select Disposable Diamonds 856-021C, Pkg/25

    Sekisui Diagnostics P.E.I. Inc.

    FDA registration
    Sekisui Diagnostics P.E.I. Inc.·47 products·🇨🇦 Canada

    Calix P PEEK Lumbar System, PLIF Rasp

    FDA Enforcement
    Class II ·Terminated·X Spine Systems Inc·October 26, 2016

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113188·PS Insert, Size 3 x 16mm

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345024113·Paddle Shaver, 16mm

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0103160·Shaver, Closed, 16mm

    PHOENIX DIGITAL EEG

    FDA 510(k)
    FDA Class 2 ·Neurology

    MERETEK UBT_LITE BREATH TEST FOR H. PYLORI

    FDA 510(k)
    FDA Class 1 ·Microbiology

    DEVICE 8252410 NIM-NEURO 2.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code IKN·February 21, 2014

    AEQ REV II GLENOID BASEPLATE DIA 25MM

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code PHX·July 1, 2025

    AEQUALIS REVERSED BASE PLATE TA6V LONG PEG WITH HA

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·March 13, 2025

    AEQ REV GLENOID BASEPLATE 29MM

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·March 6, 2025

    STRETCHER OBS 5/97

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·March 25, 2013

    OPMI PENTERO

    FDA Adverse Event
    Other ·CARL ZEISS SURGICAL GMBH·Product code EPT·March 11, 2011

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·March 26, 2008

    AEQUALIS REVERSED MULTIDIRECTIONAL GLENOID PLATE HA

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·March 25, 2024

    D.4,5MM COMPRESSION SCREW L.32MM

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·January 7, 2025