BEUDAMED
    29 results · 22ms · 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 ×

    CONTIPLEX D CONTINUOUS NERVE BLOCK SET, MODEL 331687, 331686, 331685, 331680

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707092827·BKT 41 F1000 SELF LIGATING 22

    BABY METZENBAUM SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896081291·BABY METZENBAUM SCISSORS CURVED BLADE

    D-Tect MT Accessory

    FDA UDI
    NEURONETICS, INC.·00850005944539·D-Tect MT Accessory is an accessory to the Neur...

    D-Tect MT Accessory

    FDA UDI
    NEURONETICS, INC.·00850005944928·D-Tect MT Accessory is an accessory to the Neur...

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807H100241171·IN-OVATION® C CCO 018/UL4&5 -9T 0A HK

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807H100241001·IN-OVATION® C Base Rx 018/UL4&5 -7T 0A 2D

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807H100241101·IN-OVATION® C Base Rx 018/UL4&5 -7T 0A 2D HK

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807H100241601·IN-OVATION® C Roncone 018/UL4&5 -10T 4A 2D

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807H100241611·IN-OVATION® C Roncone 018/UL4&5-10T 4A 2D HK

    RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR

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

    PROTRACT PRESS FIT HIP STEM-HA COATED

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AXLE SMALL

    FDA Adverse Event
    Malfunction ·LIMACORPORATE S.P.A·Product code JDB·August 29, 2022

    AXLE SMALL

    FDA Adverse Event
    Malfunction ·LIMACORPORATE S.P.A·Product code JDB·August 30, 2022

    VERCISE GENUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·March 1, 2024

    XIENCE SIERRA

    FDA Adverse Event
    Death ·ABBOTT VASCULAR·Product code NIQ·March 16, 2020

    PERCLOSE PROSTYLE SUTURE-MEDIATED CLOSURE AND REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·February 13, 2023

    PINNACLE PELVIC FLOOR REPAIR KITS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 8, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·September 18, 2014

    RECOVERY FILTER SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·May 16, 2011