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

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    TOXO IGG ELISA TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295242239·SIGMA TIBIAL INSERT ROTATING PLATFORM TC3 SIZE ...

    CHARNLEY

    FDA UDI
    DEPUY INTERNATIONAL LTD·10603295242246·CHARNLEY STEM FLANGED 45 22.225mm OD HEAD CEMENTED

    Westmed Gas Sampling Cannula with O2 delivery

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GRANDIO FLOW TRY-IN

    FDA 510(k)
    FDA Class 2 ·Dental

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·February 15, 2023

    PFC*SIGMA/OV/DOME PAT 3PEG,35

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 20, 2021

    SIGMA FEM ADAPTER 5 DEGREE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 20, 2021

    TC3 RP TIBIAL INSERT S3,15.0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·December 20, 2021

    UNIVERSAL STEM 75X16MM FLUTED

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 20, 2021

    UNIVERSAL STEM 75X12MM FLUTED

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 20, 2021

    SIG FEM ADAP +2/-2 OFFSET BOLT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 20, 2021

    PFC*SIGMA TC3 FEM RT SZ3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 20, 2021

    MBT REVISION CEM TIB TRAY S2.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·December 20, 2021

    PFC*SIGMA DIS AUG 4MM,SZ3,RGHT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 20, 2021

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·February 14, 2013

    UNKNOWN DEPUY LCS PATELLA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HTG·January 7, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·July 26, 2024

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EFB·September 17, 2025