BEUDAMED
    30 results · 22ms · Sources: EU EUDAMED, US FDA

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    MEDTRONIC PS MEDICAL MURPHYSCOPE, MODELS 2125-032, 2125033,2125-042, 2125-043, 2125-157, 2125-158,2125-161 2125-162,,

    FDA 510(k)
    FDA Class 2 ·Neurology

    Endo Carry-on Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964150104·Endo Carry-on Procedure Kit Includes Basin, Spo...

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·H65890103410·Zirlux Multi-Unit Abutment 3.5 mmH compatible w...

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091010341·Living mould chart Polystar HK in shade A3 cont...

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0100410·Caddie Lid, Curved Rods

    6.5MM TI RECON SCREW WITH T25 STARDRIVE 85MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MEZZOVICO·Product code HSB·April 4, 2017

    SLT DIFFUSER FIBER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DR5000 DEDICATED CHEST X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    6.5MM TI RECON SCREW WITH T25 STARDRIVE 85MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MEZZOVICO·Product code HSB·April 4, 2017

    LINER: MPACT FLAT PE HC LINER 36/G

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·September 7, 2021

    BD VACUTAINER® K2E 3.6MG PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·July 10, 2023

    RUSCH GREENLITE DISP MTL MAC 4

    FDA Adverse Event
    Malfunction ·Product code CCW·October 5, 2021

    RUSCH GREENLITE DISP MTL MAC 4

    FDA Adverse Event
    Malfunction ·Product code CCW·October 5, 2021

    Microstream SMART CAPNOLINE PLUS O2 LONG 100 UN Part Number: 010341 010341 Part Number: 10341

    FDA Recall
    Terminated ·Oridion Medical·Product code cck·May 26, 2010

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 11, 2007

    SYNVISC (HYLAN G-F 20) INJECTION

    FDA Adverse Event
    Other ·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·March 14, 2013

    EP IMPLANT TRAY

    FDA Adverse Event
    AVID MEDICAL INC·Product code LRP·February 17, 2011

    RUSCH GREENLITE DISP MTL MAC 4

    FDA Adverse Event
    Malfunction ·Product code CCW·October 5, 2021

    BD VACUTAINER® K2E PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·October 31, 2023

    BD VACUTAINER® K2E 3.6MG PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·October 25, 2023