BEUDAMED
    28 results · 23ms · Sources: EU EUDAMED, US FDA

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    REPROCESSED SURGICAL ELECTRIC INSTRUMENT

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

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694002561·2 x 4 Hole Quad Plate

    RIVA Pedicle Screw System

    FDA UDI
    XENIX MEDICAL LLC·00840493418780·CONSTRAINED LORDOTIC ROD, 6.0mm x 40mm

    RIVA Posterior Fixation System

    FDA UDI
    XENIX MEDICAL LLC·00840493418575·CONSTRAINED LORDOTIC ROD, 5.5mm x 40mm

    Restore

    FDA UDI
    KEYSTONE DENTAL, INC.·D768L12004010K0·Drill

    LATEX PRE-POWDERED EXAMINATION GLOVES WITH PROTEIN CLAIM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BIOHARNESS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024116634·

    Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024637443·

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 31, 2023

    2520274-2013-02728

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·May 20, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 25, 2014

    UNKNOWN ZIMMER HIP

    FDA Adverse Event
    Injury ·ZIMMER INC.·Product code JDI·June 7, 2011

    TREK¿

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code LOX·January 7, 2026

    HANDPIECE MICS

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·January 7, 2019

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDI·February 15, 2013

    HANDPIECE MICS

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·March 21, 2019

    HANDPIECE MICS

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·July 2, 2018

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·December 13, 2019

    HANDPIECE MICS

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·October 15, 2019