BEUDAMED
    38 results · 27ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    AZTREONAM 30 MCG. SENSI-DISC

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWT·September 8, 2022

    P.F.C.

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295216599·P.F.C. CALIBRATED PATELLAR CUTTING GUIDE

    865034

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·June 29, 2015

    AMERICAN HISTO-ID SYS PRIMARY KIT PSA PROSTATE ANT

    FDA 510(k)
    FDA Class 1 ·Pathology

    FOREMOST LITE CURE PIT & FISSURE SEALANT

    FDA 510(k)
    FDA Class 2 ·Dental

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HWT·May 5, 2016

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWT·November 17, 2023

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWT·January 10, 2020

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWT·January 10, 2020

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWT·January 17, 2018

    TOTAL ASR ACET IMP SIZE 52

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

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·October 5, 2010

    COSYCOT INFANT WARMER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code FMT·September 30, 2010

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·March 22, 2016

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HWT·November 7, 2016

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code HWT·April 8, 2016

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HWT·September 19, 2016

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·December 9, 2015

    PFC*CALIBRATED PAT CUT GDE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·August 17, 2016