BEUDAMED
    11 results · 23ms · Sources: EU EUDAMED, US FDA

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    BIOFOAM Bone Wedge

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814213·GENUMEDI PT SILVER L IV

    MiniSPC Button

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071150129·14F x 2.7cm MiniSPC Low Profile Suprapubic Cath...

    MiniSPC Button

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071147501·14F x 2.7cm MiniSPC Low Profile Suprapubic Cath...

    POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MODIFICATION TO COULTER LH 500 HEMATOLOGY ANALYZER

    FDA 510(k)
    FDA Class 2 ·Hematology

    COULTER LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·March 31, 2016

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 24, 2013

    DELTA CER HEAD 12/14 36M +5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code LZO·June 23, 2011

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·August 26, 2008

    VARIABLE SELF-DRILLING SCREW DIAM. 4X14MM (2X)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·October 4, 2017