BEUDAMED
    10 results · 20ms · 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 ×

    MC 300* Nebulizer

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Ponto

    FDA UDI
    Oticon Medical AB·05712149013913·Ponto Soft band, yellow

    HEMOSIL FIBRINOGEN-C

    FDA 510(k)
    FDA Class 2 ·Hematology

    SEEKER CROSSING SUPPORT CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BALL HEADS: COCR BALL HEAD 12/14 Ø 28 SIZE M 0

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·September 6, 2024

    SWEET TIP

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 23, 2011

    PENTERO

    FDA Adverse Event
    Malfunction ·CARL ZEISS MEDITEC, INC.·Product code EPT·June 6, 2013

    DELTEC COZMO INSULIN PUMP

    FDA Adverse Event
    Injury ·SMITHS MEDICAL MD (FORMERLY DELTEC, INC)·Product code LZG·September 22, 2008

    MPACT DOUBLE MOBILITY ACETABULAR SHELL 52

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·August 25, 2021

    LINER: MPACT DM DOUBLE MOBILITY HC LINER 28/DMG

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·September 19, 2019