BEUDAMED
    28 results · 22ms · Sources: EU EUDAMED, US FDA

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    GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    UNKNOWN PRODUCT - SET SCREW

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012

    EVOTECH™

    FDA UDI
    ADVANCED STERILIZATION PRODUCTS SERVICES INC.·10705037067213·Channel Connector Tube, White and Green

    ACRY NATURE AFG 6 LOWER

    FDA UDI
    DENTAL MANUFACTURING SPA·08056865155647·

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481115820·Attachment System, 5.0mm/5.5mm/6.5mm Internal T...

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481123030·LOCATOR F-Tx Abutment for 5.0mm PrimaConnex Int...

    CONTOURS LAPIDUS PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PLAYTEX DEODORANT TAMPONS, MODEL 34902

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

    Widex

    FDA UDI
    Widex A/S·05706069394283·Widex TV-Base (DEX silver US only ) TV-Base

    SCISSORS INSERT CEV605G 3PK 350MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S.·Product code GEI·August 29, 2013

    SCISSORS INSERT CEV605G 3PK 350MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S.·Product code GEI·August 29, 2013

    BIPOLAR INSERT CEV634-1A 350MM MOUIEL

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S.·Product code GEI·August 29, 2013

    SPECTRANETICS QUICK-CROSS SUPPORT CATHETER

    FDA Adverse Event
    Injury ·THE SPECTRANETICS CORPORATION·Product code DQY·March 6, 2019

    SCISSORS INSERT CEV605G 3PK 350MM [MXI/XOM]

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S·Product code GEI·August 15, 2013

    VENTED AUTOFEED CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·October 17, 2012

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 20, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 25, 2014

    SOLETRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·June 6, 2011

    ADULT DUAL-HEATED BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·February 19, 2013

    NEOPUFF INFANT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTL·June 5, 2012