BEUDAMED
    32 results · 27ms · Sources: EU EUDAMED, US FDA

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    WHITE MTA MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    ROLLO 110X25X12I*31*PRINTER

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763004622·

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·H65890110090·Zirlux UCLA Plastic Abut N Eng

    Ovation Hip Stem

    FDA UDI
    Ortho Development Corporation·00822409011162·EXT Size 9 Stem Plasma Spray

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193106359·HA PEEK EVOS Straight, ,9mmx11mmx 30mm , FLAT ...

    Single Use Biliary Stent V

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170185977·Single Use Biliary Stent V

    Kalitec Special

    FDA UDI
    Kalitec Direct LLC·B073DRK0100090·Dilator Sleeve, Screwdriver

    INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FHW·March 13, 1997

    KOKO PEAK KP; KOKO PEAK KP+

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RANDOX C-REACTIVE PROTEIN

    FDA 510(k)
    FDA Class 2 ·Immunology

    BD SAFETYGLIDE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMI·September 17, 2025

    BD NEEDLE ECLIPSE 25X5/8

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·February 28, 2024

    BD NEEDLE ECLIPSE 25X5/8

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·February 28, 2024

    BD NEEDLE ECLIPSE 25X5/8

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·February 28, 2024

    BD NEEDLE ECLIPSE 25X5/8

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·February 28, 2024

    BD NEEDLE ECLIPSE 25X5/8

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·February 28, 2024

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·January 27, 2012

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code MNI·April 16, 2013

    INTERFACE RESPONSE 2.0 INCREMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·March 14, 2013

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·March 8, 2011