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

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    Filters Regulation: Us FDA ×

    PDO Absorbable Punctum Plug

    FDA 510(k)
    FDA Unclassified ·Unknown

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517566232·CoRoent Ant TLIF PEEK, 15x10x28mm 8°

    Oticon

    FDA UDI
    Oticon A/S·05707131287175·RIA2 PRO, DESIGNRITE 10 WL SIL

    NEOMED ENTERAL ONLY EXTENSION SET

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    FEMVUE SALINE-AIR DEVICE

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

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 25, 2021

    ORTHOPEDIATRICS BLADE PLATE

    FDA Adverse Event
    Injury ·ORTHOPEDIATRICS·Product code HRS·October 4, 2017

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 22, 2020

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 7, 2014

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORP·Product code MVK·May 29, 2013

    LIFEPAK 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·June 7, 2011

    HUDSON ET TUBE, HVT, 8.0

    FDA Adverse Event
    Injury ·TELEFLEX MEDICAL·Product code BTR·November 19, 2021