BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    STORZ D4600 AIR EXCHANGE LINE PACK

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295241249·P.F.C. SIGMA TIBIAL INSERT ROTATING PLATFORM ST...

    NIO 5MP-M-21 (NIO 5MP MAMMO); MDNG-5121 BB

    FDA 510(k)
    FDA Class 2 ·Radiology

    ExSpiron 1Xi

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·January 24, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·January 17, 2011

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·July 28, 2014

    PFC SIGMARP STB TB IN 3 10.0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·December 29, 2021

    PFC SIGMARP STB TB IN 3 10.0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·July 8, 2020

    PFC*SIGMA/RD/DOME PAT 3PEG,38

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 29, 2021

    Depuy P.F.C. E RP Knee System Rotating Platform Stabilized Tibial Insert (RP-STAB), 10 mm, Size 3, UHMWPE, sterile; Product Code/REF 96-2131.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·September 27, 2007