BEUDAMED
    14 results · 24ms · 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 ×

    The Belmont Hyperthermia Pump

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699427·GENUMEDI SILVER SIZE VIII

    SAFE-T PLUS THORACENTESIS/PARACENTESIS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code GCB·March 16, 2020

    5 FR NON-VALVED THORA/PARA TRAY

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code GCB·March 11, 2020

    2.0 LACTOSORB SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036054779·

    GLUCOSE PILOT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NANOGEN

    FDA 510(k)
    FDA Class 2 ·Dental

    AMISTEM H HA COATED STD STEM SIZE 1

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·November 9, 2018

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 7, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 23, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 10, 2008

    2.0 LACTOSORB SYSTEM 2.0 X 7 MM DIRECT DRIVE SCREW

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HWC·April 30, 2021

    2.0 LACTOSORB SYSTEM 2.0 X 7 MM DIRECT DRIVE SCREW

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HWC·January 5, 2021

    ELEKTA LIMITED Elekta Synergy, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear

    FDA Enforcement
    Class II ·Ongoing·Elekta, Inc.·December 13, 2023