BEUDAMED
    25 results · 21ms · Sources: EU EUDAMED, US FDA

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    CAMPYLOBACTER SUPPLEMENT -SKIRROW

    FDA 510(k)
    FDA Class 1 ·Microbiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699588·GENUMEDI PSS BLUE, SIZE VI

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981124083·18x15x6mm, 7 Degree, No Profile Integrated Spacer

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·00889981124086·No Profile Spacer, 18x15x6mm, 7 Degree, Sterile

    Chex-All Sterilization Pouches and Tubes

    FDA 510(k)
    FDA Class 2 ·General Hospital

    D2RS_AT Digital Dynamic Remote System

    FDA 510(k)
    FDA Class 2 ·Radiology

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Product code NPZ·March 27, 2013

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Product code NPM·March 28, 2013

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015