BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Nalu Lead Blank (50cm)

    FDA 510(k)
    FDA Class 2 ·Neurology

    VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184,

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SUPRAMID BLACK 4/0 (1.5) 45CM DS19

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAR·September 12, 2019

    PINNACLE SECTOR II CUP 52MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·March 6, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    CRYSTALLINE ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·August 8, 2014