BEUDAMED
    15 results · 32ms · Sources: EU EUDAMED, US FDA

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    EXTENDED MALAR IMPLANT

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257073445·PROTECT PATELLA TRACKING BRACE, LT, 2X

    DD tempMED

    FDA UDI
    Dental Direkt GmbH·EDDIK115151·DD tempMED are pre-colored dental milling blank...

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909115152·REVELATION DIAMOND SE6-016VF - 5 PACK

    "1.5MM" SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036053321·

    MEDLINE GROUNDING PAD

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

    SPSMEDICAL SPORVIEW STEAM BI

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DUROM ACETABULAR COMPONENT

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·May 27, 2014

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013

    KARL STORZ DEBAKEY

    FDA Adverse Event
    Malfunction ·KARL STORZ·Product code GCJ·November 19, 2010

    "1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·April 2, 2019

    "1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·April 10, 2019

    "1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·August 3, 2018

    PRODISC-L TRIAL-IMPL L 9° 10

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code MJO·January 15, 2019

    VITEK® 2 AST-GP75 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·February 12, 2018