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

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    CONDOM-52.XX

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

    LMDental

    FDA UDI
    LM-Dental·06438311220765·LM-LiftOut S5, Extraction

    Cortera

    FDA UDI
    Xtant Medical Holdings, Inc.·00840311234059·Tap, NAV, Open Cann, 12.5

    CHX=CHX PLUS

    FDA 510(k)
    FDA Unclassified ·Unknown

    RAICHEM MULTI-ANALYTE CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    REALSEAL

    FDA Adverse Event
    Injury ·SYBRONENDO·Product code KIF·May 15, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    INRATIO

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code GJS·August 20, 2010

    COMP RVS CNTRL 6.5X20MM ST/RST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 12, 2020

    COMP LK SCR 3.5HEX 4.75X15 ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 12, 2020

    COMP LK SCR 3.5HEX 4.75X20 ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 12, 2020

    COMP LK SCR 3.5HEX 4.75X15 ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 12, 2020

    COMPREHENSIVE REVERSE BASEPLATE HA+ADAPTER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 11, 2019

    E1 COMPREHENSIVE HUMERAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 11, 2019

    COMPREHENSIVE REVERSE SHOULDER GLENOSPHERE STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 11, 2019

    Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089; CD1235-40/100029272, 100029282, 100029311, 100031039, 100059779; CD1235-40Q/100029273, 100029295, 100029312, 100030840; CD1241-40/100046351; CD1241-40Q/100046167; CD2231-40/100029274, 100030110, 100041922; CD2231-40Q/100029275, 100030089, 100041923; CD2233-40/100029147, 100029276, 100029313, 100031066, 100037043, 100048759, 100070007; CD2233-40Q/100029148, 100029263, 100029314, 100031067, 100037044, 100059770, 100070068; CD2235-40/100029149, 100029265, 100029283, 100031029, 100059837; CD2235-40Q/100029239, 100029258, 100029284, 100031030, 100066504; CD2241-40/100046148; CD2241-40Q/100046149; CD2299-40/100056952

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018