BEUDAMED
    17 results · 19ms · Sources: EU EUDAMED, US FDA

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    SONICATOR PLUS 992, MODEL NUMBER ME 992 AND SONICATOR PLUS 994, MODEL NUMBER ME 994

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984142·anteriors; shade A3.5; mould R 55

    P.F.C.

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295252320·P.F.C. TIBIAL INSERT FIXED BEARING CURVED 2 8mm...

    OXINET N-7500 PULSE OXIMETRY NETWORK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ULTRANET-S COLLIMATOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·December 13, 2013

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·January 8, 2014

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·May 12, 2015

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·September 6, 2012

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 24, 2013

    BIA400 IMPLANT 4MM W ABUTMENT 8MM

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·May 25, 2016

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·April 1, 2013

    LD304 MATERNITY BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code HDD·February 28, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·February 10, 2011

    EMAX 2 MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 18, 2013

    Bentson Wire Guide

    FDA Enforcement
    Class II ·Terminated·Cook Inc.·March 21, 2018

    Depuy P.F.C. Modular Knee System, curved tibial insert (CVD); polyethylene tibial insert, Sz 2, 8.0 mm; Ref 98-4142.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code JWH·May 26, 2005