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

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    CONSTRUX Mini PEEK Spacer System, CONSTRUX Mini PEEK Ti Spacer System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Leg Bag

    FDA UDI
    C. R. Bard, Inc.·00801741050831·Dispoz-A-Bag, Leg Bag with Flip-Flo Drainage Va...

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171028161·PESSARY, DISH #6, W/O SUPPORT, 80mm

    KING SEPTEMS

    FDA Adverse Event
    Malfunction ·KING SEPTEMS·Product code LMA·November 1, 2012

    SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827

    FDA 510(k)
    FDA Class 2 ·Radiology

    20.8-INCH (53CM) COLOR LCD MONITOR, MODELS CDL2112A, CCL350I & DV3MC-HB

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·March 31, 2020

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 6, 2013

    TI CLICK'X LOCKING CAP FOR TI 3-D HEAD

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code NKB·June 24, 2011

    TREVO XP PROVUE 4MM X 30MM

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code NRY·July 24, 2020

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·March 10, 2020

    KING LAD SILI CONE SINGLE USE, King Systems, 10 devices/case, ETO Sterile Size 4 / Adult Silicone King LAD¿ Patient Size: 50-70kg

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012