BEUDAMED
    46 results · 24ms · Sources: EU EUDAMED, US FDA

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    KROM-ALGINATE AND ALGINATE PLUS

    FDA 510(k)
    FDA Class 2 ·Dental

    PowerPICC Provena

    FDA UDI
    Bard Access Systems, Inc.·00801741137709·Catheter Placement Kit

    S NEEDLE

    FDA UDI
    asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282505264·asia-med s-needle J-Type 2050 Place N' Press: c...

    S NEEDLE

    FDA UDI
    asia-med GmbH·04251282512255·asia-med s-needle J-Type 2050 Place N' Press: c...

    Non-Telescopic PenEvac® MaxReveal ™ Diamond Crystal®

    FDA UDI
    I.C. MEDICAL, INC.·00817688023982·Non-Telescopic PenEvac® MaxReveal ™ Diamond Cry...

    APPLIANCE, FIXATION, NAIL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KTT·August 18, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 5, 2016

    DATEX-OHMEDA INOVENT DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    WILSON-COOK REUSABLE HOT BIOPSY FORCEPS

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

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES BETTLACH·Product code HWC·September 23, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES MEZZOVICO·Product code HWC·September 1, 2015

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 3, 2023

    SCREW LOCKING

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES OBERDORF·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    LCP 4.5/5 BROAD 18HO L332 TI

    FDA Adverse Event
    Injury ·SYNTHES·Product code KTT·December 12, 2012

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·March 12, 2013

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - GUANGZHOU·Product code KDJ·February 24, 2011