BEUDAMED
    108 results · 26ms · Sources: EU EUDAMED, US FDA

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    BIOPTRON PRO LIGHT THERAPY SYSTEM AND BIOPTRON COMPACT III LIGHT THERAPY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526785533·M4S COMFORT COMPACT BLACK LEFT XXL

    Baltic Denture System BD Load

    FDA UDI
    Merz Dental GmbH·D7091032216·Baltic Denture System BDLoad Mm6 PLSEbim6DFm A2...

    Battalion

    FDA UDI
    ALPHATEC SPINE, INC.·00840967187648·Battalion, LLIF Trial, 15°, 22 mm Wide, 16 mm X...

    NITRILE EXAMINATION GLOVE, PRE-POWDERED, COLOR WHITE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NIROYAL BILIARY PREMOUNTED STENT SYSTEM

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

    SCP PANEL CENTRIFUGE JMS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·November 5, 2013

    SM FRAG LCP INSTR/IMPL SET GRAPHIC CASE W/O SCR RACK

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code FSM·April 3, 2013

    REALIZE LAP-BAND

    FDA Adverse Event
    Malfunction ·ETHICON·Product code LTI·February 4, 2011

    SYNCHRO 2/14 200 CM STANDARD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQX·April 18, 2008

    S4 IMPLANTS

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code KWP·August 29, 2008

    SCP PANEL CENTRIFUGE JMS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·March 14, 2014

    SCP CONTROL PANEL

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012

    CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DWA·January 19, 2018

    CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND GMBH·Product code DWA·January 5, 2022

    STOCKERT JMS CENTRIFUGAL PUMP SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012

    MONOPLUS VIOLET 0 (3,5) 90CM HR37S(M)RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.U.·Product code NEW·December 14, 2021

    MONOPLUS C VIOLET 2/0 (3) 25M

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·January 2, 2019

    MONOPLUS VIOLET 4/0 (1.5) 70CM HR17 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·October 23, 2019

    STOCKERT CENTRIFUGAL PUMP (SCP) SYSTEM

    FDA Adverse Event
    Injury ·SORIN GROUP DEUTSCHLAND·Product code DWA·May 7, 2010