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

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    ACON MOP ONE STEP OPIATE TEST STRIP, ACON MOP STEP OPIATE TEST DEVICE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Affinity™ Heavy Body RS Mega Mix 380ml

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172000130·VPS Impression Material

    Affinity™ Heavy Body RS Mega Mix 380ml

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172017039·VPS Impression Material

    AOS MODULAR NAIL 13.0mm x 38cm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665003338·

    STEVE MADDEN

    FDA UDI
    FGX INTERNATIONAL INC.·00193033483138·

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310K0133000·Assembly, Rod Reducer, Ratcheting

    BIOTEQUE VAGINAL DILATOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MP3HD BIG BOY, POWER WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    FR CLERMONT FERRAND

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 3, 2012

    MERCY HSP PITTSBURGH PA 1

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DWE·May 7, 2009

    HCSG/HENDRICK MED/ABLNE TX 1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code DWE·February 16, 2010

    DIDECO COMPACTFLO EVO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·January 16, 2013

    DIDECO COMPACTFLO EVO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code KFM·December 13, 2012

    DIDECO COMPACTFLO EVO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 18, 2012

    OT SELECT METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 20, 2013

    TRABECULAR METAL PRESS FIT FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LPH·March 8, 2011

    KAPPA 700 DR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·March 10, 2008

    OPTILENE 6/0 (0,7) 75CM 2XDRC10 CV RCP

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAW·December 6, 2019

    OPTILENE 6/0 (0,7) 45CM DS16 (M) RCP

    FDA Adverse Event
    Malfunction ·B/ BRAUN SURGICAL SA·Product code GAW·July 22, 2019

    OPTILENE 6/0 (0,7) 45CM DS16 (M) RCP

    FDA Adverse Event
    Malfunction ·B/ BRAUN SURGICAL SA·Product code GAW·July 22, 2019