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

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    THE MONITOR ELECTRONIC BED ALARM SYSTEM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    VuePoint

    FDA UDI
    Nuvasive, Inc.·00887517174079·VuePoint Screw, 3.5x30mm Polyaxial Tulip

    OnBrace Crown UL7 (5/pk)

    FDA UDI
    SPECIALTY APPLIANCES, LLC·D8199013300·

    INTEGRATED NEEDLEHOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09929013300·NEEDLEHOLDER WITH TUNGSTEN CARBIDE INSERTS CROS...

    NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896100527·NEEDLE HOLDER SINGLE ACTION STRAIGHT JAW TUNGST...

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918143972·Alleset Gown_W/reinforcement_X-Large_Non-steril...

    SOVEREIGN BIPOLAR INSTRUMENTS

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

    MIDWEST REPROCESSING CENTER REPROCESSED SCD EXPRESS SLEEVES/ FOOT CUFFS, MIDWEST REPROCESSING CENTER REPROCESSED ALP SLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918192840·Alleset Gown_W/fabric reinforcement_X-Large_W/ ...

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·March 10, 2021

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·March 22, 2021

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·May 31, 2021

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 30, 2014

    PREFYX PPS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code FTL·January 8, 2013