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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    BARDEX LUBRI-SIL I.C. FOLEY CATHETER

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

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984136·anteriors; shade A3.5; mould Q 46

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122987·K-WIRE - SINGLE TROCAR 1.25mm DIA x 150mm

    WORLD CHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    SUTURE TENSION ADJUSTMENT REEL

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ETEST FOSFOMYCIN FM 1024 WW B30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code JWY·April 16, 2020

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·February 28, 2013

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·August 6, 2014

    AXIUM 3-D DETACHABLE COIL

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code HCG·February 10, 2011