BEUDAMED
    238 results · 23ms · Sources: EU EUDAMED, US FDA

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    3Shape Splint Design

    FDA 510(k)
    FDA Class 2 ·Dental

    Oticon

    FDA UDI
    Oticon A/S·05707131339959·SIYA 1, KIT IIC 10 85 C005

    IMMUKNOW-THE CYLEX IMMUNE CELLFUNCTION ASSAY

    FDA 510(k)
    FDA Class 2 ·Hematology

    BOLUS COMPENSATOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 10, 2025

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 11, 2025

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·October 1, 2008

    PEDICSCR PANGEAPOLYAX Ø6 CANN PREASSMBL

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code NKB·June 27, 2013

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code LZS·July 22, 2011

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 11, 2026

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 7, 2026

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 3, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 5, 2025

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B.BRAUN MELSUNGEN AG·Product code FRN·April 30, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 13, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 14, 2026

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 1, 2025

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 11, 2026

    COCHLEAR OSIA OSI300 IMPLANT

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code PFO·March 8, 2026