BEUDAMED
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    Filters Status: Malfunction ×

    LIGHTMIX ZIKA RRT-PCR TEST (EUA)

    FDA Adverse Event
    Malfunction ·OLFERT LANDT, TIB MOLBIOL SYNTHESELABOR GMBH·Product code POA·March 9, 2017

    LIGHTMIX ZIKA RRT-PCR TEST (EUA)

    FDA Adverse Event
    Malfunction ·OLFERT LANDT, TIB MOLBIOL SYNTHESELABOR GMBH·Product code POA·March 9, 2017

    TRUSCAN BODY COMPATIBLE WITH HIOSSEN (OSSTEM) ET (TS) REGULAR

    FDA Adverse Event
    Malfunction ·TRUABUTMENT KOREA CO., LTD.·Product code NDP·February 4, 2025

    CARDIOSAVE

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·June 3, 2014

    ELLIPSE VR ICD, US

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. (CRM-KISTA)·Product code LWS·September 2, 2015

    SENSATION PLUS UNK.VOL

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DSP·July 10, 2017

    ACCURA HEMOFILTRATION SYSTEM

    FDA Adverse Event
    Malfunction ·MESYS·Product code FIR·November 27, 2007

    ACCURA HEMOFILTRATION SYSTEM

    FDA Adverse Event
    Malfunction ·MESYS GMBH- MEDIZINISCHE SYSTEME·Product code FIR·May 19, 2008

    BM14 FLUID UF MODULE FOR BM25

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES GERMANY GMBH·Product code FIR·June 22, 2011

    MAYFIELD TRIAD SKULL CLAMP

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·July 9, 2013

    AMK CEM FIX STEM TIB TRAY

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·March 15, 2002

    TRIGEN FEMORAL INTRAMEDULLARY NAIL

    FDA Adverse Event
    Malfunction ·SMITH AND NEPHEW, INC.·Product code JDS·February 28, 2022

    CORE UNIVERSAL DRIVER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HBE·May 18, 2012

    BARD

    FDA Adverse Event
    Malfunction ·BARD·Product code LJT·July 28, 2004

    UNKNOWN SPINAL CORD STIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·April 22, 2010

    DELUXE POSTERIOR VITRECTOMY PACK

    FDA Adverse Event
    Malfunction ·STORZ OPHTHALMICS, INC.·Product code KYG·June 27, 1997

    ARROW RADIAL ARTERY CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL, INC.·Product code DQO·January 17, 1996

    ENDO GIA ULTRA

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GDW·December 18, 2018

    GUGLIELMI DETACHABLE COIL POWER SUPPLY

    FDA Adverse Event
    Malfunction ·TARGET THERAPEUTICS / A DIV. OF BOSTON SCIENTIFIC CORP.·Product code HCG·June 9, 1999

    ETS 35 ENDO LIN CTTR WHT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code KOG·April 27, 2005