BEUDAMED
    269 results · 29ms · Sources: EU EUDAMED, US FDA

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    BracePaste MTP Light Cure Primer

    FDA 510(k)
    FDA Class 2 ·Dental

    Monoject

    FDA UDI
    Cardinal Health 200, LLC·10192253024968·Hypodermic Safety Needle 19G x 1" (1.1 x 25 mm)

    Monoject

    FDA UDI
    Cardinal Health, Inc.·10884521544741·Hypodermic Safety Needle

    Vanguard Select Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304555501·

    IN-OVATION® R

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K189110001·IN-OVATION® R TGO 020X028 UL/5-5 CS-BC HK

    3M ATTEST RAPID READOUT STEAM PROCESS CHALLENGE DEVICE, MODEL 1296V, 3M ATTEST RAPID READOUT STEAM-PLUS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NON-STERILE, POWDERED LATEX EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 16, 2012

    UNKNOWN DEPUY FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KXA·December 6, 2012

    STAB HIP PC 12-20 MD W/CS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code MEH·January 17, 2013

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code JDI·November 8, 2012

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD 8010379·Product code KWA·December 11, 2014

    S-ROM M HEAD 36MM +3

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD 8010379·Product code LPH·December 30, 2014

    PINNACLE MTL INS NEUT36IDX50OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 21, 2013

    UNKNOWN DEPUY FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KXA·January 2, 2013

    UNKNOWN DEPUY ASR XL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·July 26, 2016

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·July 26, 2016

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·May 12, 2016

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·May 12, 2016

    ADAPTER SLEEVES 12/14 +5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·May 12, 2016