BEUDAMED
    14 results · 18ms · Sources: EU EUDAMED, US FDA

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    HYCOR HY.TEC/MANUAL JO-1 AUTO-ANTIBODY

    FDA 510(k)
    FDA Class 2 ·Immunology

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295244066·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING STABIL...

    ELITE

    FDA UDI
    DEPUY (IRELAND)·10603295244073·ELITE FEMORAL HEAD +3 9/10 TAPER Diameter 22.225mm

    STA-SOF BREAST COMPRESSOR-CLAMP

    FDA 510(k)

    ULTRASONIC SCALER, VARIOS 560

    FDA 510(k)
    FDA Class 2 ·Dental

    E.COM, SYMBIA E

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code IYX·March 15, 2012

    E.CAM

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code KPS·January 7, 2014

    SYMBIA T-SERIES

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code KPS·September 20, 2013

    E. CAM COMPUTER [510(K) K992731]

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC.·Product code IYX·April 20, 2001

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 22, 2010

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·February 14, 2013

    SINGLE TRIGGER ROTARY

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HWE·July 29, 2014

    Depuy P.F.C. E Knee System, stabilized plus tibial insert (STAB PLUS); polyethylene tibial insert, Sz 3, 12.5 mm; Ref 96-2731.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005

    Depuy P.F.C. E Knee System Stabilized Plus Tibial Insert (STAB PLUS), 71 mm M/L, 47 mm A/P, 12.5 mm, 3, UHMWPE, sterile; Product Code/REF 96-2731.

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