BEUDAMED
    49 results · 21ms · 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.

    HEMOSTATIX, MODEL 2400Z THERMAL SCALPEL SYSTEM

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

    Baltic Denture System BD Load

    FDA UDI
    Merz Dental GmbH·D7091033089·Baltic Denture System BDLoad ↓ Sw6 PLSEum6DFs D...

    GELSPHERES EMBOLIC AGENT

    FDA 510(k)
    FDA Class 2 ·Neurology

    EMS HEPA FILTER AND HME COMBINATIONS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PS CONSTRAINED INSERT XLG

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code JWH·July 20, 2017

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 1, 2013

    CARDIOVASCULAR PROCEDURE KIT

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code OEZ·February 28, 2011

    UNK DEPUY LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·April 22, 2008

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 7, 2025

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 6, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 7, 2025