BEUDAMED
    13 results · 22ms · 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 ×

    Ballancer 505 System, Model 1201-AC

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Oticon

    FDA UDI
    Oticon A/S·05707131286666·RIA2 PRO, RITE 312 WL CNB

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756319799·150 ML W/FILL TUBE LF 6000

    Femoral Trial Size 4N

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215073688·

    NOVATION CROWN CUP GXL LINERS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    U1 HIP SYSTEM - BIPOLAR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEROYAL

    FDA Adverse Event
    Other ·COEUR LABORATORIES, INC.·Product code DXT·July 10, 2012

    ANGIOMAT ILLUMINA

    FDA Adverse Event
    Malfunction ·MALLINCKRODT INC., LIEBEL-FLARSHEIM BUSINESS·Product code DXT·June 5, 2012

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·May 29, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 10, 2011

    UHN Ø6.7 L220 TAN VIOL

    FDA Adverse Event
    Malfunction ·SYNTHES SALZBURG·Product code HWC·October 14, 2015

    WAVEWRITER ALPHA? PRIME 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 4, 2024

    150 ML W/ FILL TUBE LF 6000

    FDA Adverse Event
    Malfunction ·COEUR, INC.·Product code DXT·January 3, 2020