BEUDAMED
    10 results · 22ms · Sources: EU EUDAMED, US FDA

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    SALTERLABS 8960 SERIES NEBULIZER (8960/8961/8966/8984)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295239093·P.F.C. SIGMA STABILIZED TIBIAL INSERT TRIAL SZ ...

    SMR Shoulder System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS06-1

    FDA 510(k)
    FDA Class 2 ·Neurology

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·February 14, 2013

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·January 9, 2011

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 28, 2014

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·March 21, 2024

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·March 26, 2018