BEUDAMED
    57 results · 22ms · Sources: EU EUDAMED, US FDA

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    Monopolar Single Use Laparoscopic Instrument

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Brasseler

    FDA UDI
    Provision·B504OMKM715230·

    NON-BR2000 LARGE BONE BLADES

    FDA UDI
    Peter Brasseler Holdings, LLC·00887919095293·KM71-523

    NA

    FDA UDI
    STERILMED, INC.·10888551017602·SAW BLADE OSCILLATING LARGE BONE

    SR MCP

    FDA UDI
    Stryker GmbH·00886385020938·S.R. MCP PHALANGEAL BROACH ASSEMBLY, LG

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071715231T20·Toothed Curette Angled Cup Left 15"

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M9307171523110·Curette, Right "9 Iron" #3 8" working length

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M9307171523120·Curette, Left "9 Iron" #3 8" working length

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071715231T10·Toothed Curette Angled Cup Right 15"

    FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR, MODELS BP1600, BP1650, BP1700 AND BP1750

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CIRCUFLOW 5200 SEQUENTIAL COMPRESSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·February 12, 2019

    INDIGO SYSTEM SEPARATOR D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·April 18, 2018

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·May 29, 2019

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·January 17, 2020

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·December 7, 2018

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·January 29, 2021

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·December 10, 2020

    PENUMBRA SYSTEM JETD REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·June 5, 2019

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·January 25, 2019