BEUDAMED
    16 results · 31ms · 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 ×

    VERTEBRAL ACCESS SYSTEM BY VIDACARE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Tiger Supply Inc.

    FDA UDI
    TIGER SUPPLY, INC.·D82360817131·VPS Impression Material Light Body Regular Set ...

    SAFESKIN NEON NITRILE - POWDER FREE NEON EXAM GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA

    FDA 510(k)
    FDA Class 2 ·Radiology

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·April 29, 2013

    CAREASSIST BED

    FDA Adverse Event
    Malfunction ·HILL-ROM PLUVIGNER·Product code FNL·April 12, 2011

    LASSO 2515 VARIABLE CIRCULAR MAPPING CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·July 4, 2008

    ULTRAXX NEPHROSTOMY BALLOON AND SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LJE·August 8, 2024

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·July 3, 2018

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·July 3, 2018

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·June 25, 2018

    Catheter, intravascular, therapeutic, short-term less than 30 days

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·November 10, 2022

    1820334-2022-00399

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·March 16, 2022

    GAM Kirschner Wire, Sterile R, T2 K-Wire, Sterile R and T2 K-Wire Recon, Stryker Trauma GmbH, Prof.-Kuntscher-Strasse 1-5, Schonkirchen, Germany 24232; T2 K-Wire, Sterile R Intended for the temporary stabilization of bone segments or fragments

    FDA Enforcement
    Class II ·Terminated·Stryker Howmedica Osteonics Corp.·December 28, 2016