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

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    SILASTIC BONE PLUG H.P.(CEMENT RESTRICT)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AUTO SUTURE ENDO GIA STAPLERS WITH ENDO GIA SINGLE USE LOADING UNITS WITH STAPLE LINE REINFORCEMENT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    EEG WITH VIDEO, MODEL EX-NW

    FDA 510(k)
    FDA Class 2 ·Neurology

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code DSP·August 1, 1998

    FUSA F80B (HF/PS/1.8/H)

    FDA Adverse Event
    Injury ·FRESENIUS·Product code KDI·May 19, 1998

    M2A 1 PC SHELL 38MMX60MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 8, 2014

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·October 18, 2012

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 16, 2010

    Creatine Kinase (CK) used on cobas c 311/501/502 and COBAS INTEGRA 400 plus-In vitro test for the quantitative determination of creatine kinase (CK) in human serum and plasma. Catalog Number: 07190794190

    FDA Recall
    Open, Classified ·Roche Diagnostics Operations, Inc.·Product code JHS·August 15, 2024