BEUDAMED
    25 results · 26ms · Sources: EU EUDAMED, US FDA

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    Powder Free Nitrile Examination Glove

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575290055·Orthopaedic chisel - Endo Model Rotational and ...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575290017·Orthopaedic chisel - Endo Model Rotational and ...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575290062·Orthopaedic chisel - Endo Model Rotational and ...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575290031·Orthopaedic chisel - Endo Model Rotational and ...

    BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS, BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS FOR PRESBYOPIA,

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OBIX PERINATAL DATA SYSTEM 7.0

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

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008034·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008041·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008058·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008065·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008072·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008089·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008096·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

    ASR ACETABULAR CUPS 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 30, 2011

    DAMON COPPER NITI WIRE

    FDA Adverse Event
    Malfunction ·ORMCO CORPORATION·Product code DZC·September 9, 2008

    Na¿da CL Q30 Sound Processor, Sand Beige, Model Cl-5260-120; Silver Gray, Model Cl-5260-140; and Velvet Black, Model Cl-5260-150.

    FDA Enforcement
    Class II ·Terminated·Advanced Bionics, LLC·April 10, 2019

    EVERCROSS 035

    FDA Adverse Event
    Injury ·COVIDIEN·Product code LIT·December 20, 2023

    METRIX AIR

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·November 29, 2017