BEUDAMED
    10,000 results · 208ms · Sources: EU EUDAMED, US FDA

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    ABC Nipple

    FDA UDI
    AMERICAN BREAST CARE, L.P.·00811749024833·Nipple prosthesis, external 906 ABC Nipple Made...

    Geminus

    FDA UDI
    SKELETAL DYNAMICS L.L.C.·00841506105529·

    AndoFlex TLC

    FDA UDI
    Andover Healthcare, Inc.·10724004614939·Two-Layer Compression Kit Layer 1 is a soft foa...

    TRI

    FDA UDI
    TRI Dental Implants Int. AG·07640149886863·

    TRI

    FDA UDI
    TRI Dental Implants Int. AG·07640149885255·

    TRI

    FDA UDI
    TRI Dental Implants Int. AG·07640149885132·

    Geminus

    FDA UDI
    SKELETAL DYNAMICS L.L.C.·00841506101613·

    Geminus

    FDA UDI
    SKELETAL DYNAMICS L.L.C.·00841506101408·

    DISC HUM 6X150MM LT FLANGED C

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·July 9, 2019

    DISC CONDYLE KIT W/ HEXALOBULA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·July 9, 2019

    MOSAIC 6.5 X 75MM IM STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWT·October 10, 2017

    COMPR SRS 60MM DST HML BDY LT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWT·March 14, 2019

    COMPREHENSIVE SRS DISTAL BODY WITH SCREW - LEFT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWT·March 6, 2018

    UNKNOWN DISCOVERY HUMERAL CONDYLE KIT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·June 20, 2018

    COMPR SRS 50MM DST HML BDY LT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWT·June 19, 2018

    UNKNOWN COMPREHENSIVE SRS MOD STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·June 20, 2018

    UNKNOWN COMPREHENSIVE SRS FLANGE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·June 20, 2018

    VITEK 2 GRAM-NEGATIVE SUSCEPTABILITY TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LTW·May 12, 2014

    VITEK 2 GRAM-NEGATIVE SUSCEPTIBILITY TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LTW·May 7, 2014

    VITEK2

    FDA Adverse Event
    Malfunction ·BIOMERIUEX·Product code LTW·February 22, 2010