BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    ACKERMANN EUROPCLIP

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

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517288370·CoRoent LC Ti, 11x9x30mm 8°

    SureFISH IGH BCL2 DF P200

    FDA UDI
    AGILENT TECHNOLOGIES, INC.·05700574008963·SureFISH IGH BCL2 DF P200

    Trocar

    FDA UDI
    SOPRO-COMEG GmbH·04059082005409·

    MEMOMETAL NAVIS BONE PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACTIVE WASTE GAS SCAVENGER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RECAP SHELL COCR PC 54/48MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·May 14, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 2, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 15, 2008

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 12, 2016

    EMBLEM S-ICD Model A209

    FDA Enforcement
    Class I ·Terminated·Boston Scientific Corporation·February 17, 2021

    INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·July 21, 2021