BEUDAMED
    13 results · 19ms · Sources: EU EUDAMED, US FDA

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    BRIGHTWAY BRAND LATEX SURGICAL GLOVES - STERILE (POWDERED)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Inrad

    FDA UDI
    Inrad·00817295020718·SelectCore Variable Throw Biopsy Device 20 ga x...

    Bioseal Inc.

    FDA UDI
    BIOSEAL·00630094992020·Graduated Triangle Pitcher

    IMA Retractor Blade & Clamp

    FDA UDI
    KOROS U.S.A., INC.·10840199542762·IMA Retractor Blade & Clamp Assembly

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110942·STERILIZING CASE PLASTIC SMALL

    AADVA ZR COLORING LIQUID

    FDA 510(k)
    FDA Class 2 ·Dental

    Celerity HP Chemical Indicator, Celerity Vaporized VH2O2 Process Indicator Adhesive Label, VERIFY V24 Self-Contained Biological Indicator Vial Label

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·March 7, 2013

    VERSA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·February 15, 2011

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·August 8, 2014

    VANGUARD DCM TIBIAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 28, 2017

    EQUINOXE REVERSE 38MM HUMERAL LINER +0

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·December 29, 2022

    HAMILTON MEDICAL AG

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·October 2, 2023