BEUDAMED
    34 results · 39ms · Sources: EU EUDAMED, US FDA

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    INTERACTIVE SBM 3.7MMDX13MML 3.0MM PLAT

    FDA Adverse Event
    Injury ·IMPLANT DIRECT SYBRON MANUFACT·Product code DZE·October 29, 2025

    INTERACTIVE/ SWISHPLUS2 IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    EVONOS

    FDA UDI
    Gyrus ACMI, LLC·00821925015036·HOUSE TYPE MEASURING ROD 4.5 MM

    PN841

    FDA UDI
    Respironics, Inc.·00606959041592·PN841, Child Large, with Standard Elbow, Japan

    MATHIEU-OLSEN NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896075832·MATHIEU-OLSEN NEEDLE HOLDER SERRATED TIP

    VERSACLOSE, MODEL VC-200-01

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

    HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·May 28, 2014

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·March 21, 2014

    SYRINGE 10ML LL BNS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 17, 2021

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·BBRAUN MEDICAL SAS·Product code LJT·July 1, 2015

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·April 11, 2014

    CELSITE

    FDA Adverse Event
    Injury ·B .BRAUN MEDICAL SAS·Product code LJT·February 20, 2017

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·September 14, 2015

    CELSITE

    FDA Adverse Event
    Injury ·B.BRAUN MEDICAL SAS·Product code LJT·April 8, 2020

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·March 21, 2014

    CELSITE

    FDA Adverse Event
    Injury ·B .BRAUN MEDICAL SAS·Product code LJT·August 3, 2017

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·July 10, 2014

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 24, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·September 30, 2014