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

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    FORTIVA PORCINE DERMIS

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

    ArgenZ ST 98x18 ML B4

    FDA UDI
    ARGEN CORPORATION, THE·D818123356·Dental porcelain/ceramic restoration kit

    Logical G-Series

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215000899·

    Logical G-Series Acetabular Shell

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215052140·

    Paxeon Logical

    FDA UDI
    PAXEON RECONSTRUCTION LLC·08177570201280·Logical G-Series Shell – 3 Holes Size 56-D

    OrthoMedFlex

    FDA UDI
    ORTHOMEDFLEX LLC·M7161111233560·56mm Acetabular Cup (3-hole)

    PRUITT CAROTID KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KLOCK WATCH STYLE DIGITAL BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VENTO Cup

    FDA UDI
    AMPLITUDE SAS·03701089514071·

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 18, 2019

    VERTEX® RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 16, 2017

    VERTEX® RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·March 3, 2017

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·October 18, 2018

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

    ECHELON*FLEX60 ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60 MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 26, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011

    VERTEX® RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·March 17, 2017

    VERTEX® RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·July 15, 2024

    BD ULTRA-FINE¿ PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FMI·March 5, 2019

    NOVATION

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code MEH·November 25, 2019