BEUDAMED
    3,546 results · 34ms · Sources: EU EUDAMED, US FDA

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    Di-Chem Hemodialysate Additive

    FDA UDI
    Di-Chem, Incorporated·B637KAC2001·Liquid potassium acetate additive for bicarbona...

    KAC-300 KNEE ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    KAC-63 KNEE ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    Welch Allyn, Inc.

    FDA UDI
    WELCH ALLYN, INC.·00732094302066·Surveyor S19 GEN1 Patient Monitoring System - N...

    MEDFUSION 3500 SYRINGE INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDEX·Product code FRN·September 22, 2006

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·August 2, 2023

    TEV WH BR 5 KAC-25 1N 24" 1/BX NICELOOP

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GAT·March 7, 2018

    TEV GN BR 5 KAC-25 1N 24" NICELOOP

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GAT·December 18, 2024

    TEV WH BR 5 KAC-25 1N 24" NICELOOP

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GAT·December 18, 2024

    UNK - SYNFLATE/VBS

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NDN·July 2, 2024

    UNK - BIOMATERIAL - CEMENT: VERTECEM V+

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NDN·July 2, 2024

    BIVONA MICROLARYNGEAL WIRE TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code KAC·February 23, 2010

    PROVOX LARYTUBE 9/36

    FDA Adverse Event
    Malfunction ·ATOS MEDICAL AB·Product code KAC·April 15, 2021

    PROVOX LARYTUBE 9/36

    FDA Adverse Event
    Malfunction ·ATOS MEDICAL AB·Product code KAC·April 9, 2021

    PROVOX LARYBUTTON

    FDA Adverse Event
    Injury ·ATOS MEDICAL AB·Product code KAC·March 19, 2014

    SUCTION TUBE MCLT50 MALLEAB BLUNT TERRIS

    FDA Adverse Event
    Malfunction ·INTEGRA MICROFRANCE S.A.S.·Product code KAC·June 28, 2019

    SHILEY

    FDA Adverse Event
    Injury ·JUAREZ HENEQUEN·Product code KAC·October 24, 2006

    PROVOX LARYTUBE 9/36, FENESTRATED

    FDA Adverse Event
    ATOS MEDICAL AB·Product code KAC·November 25, 2016

    PROVOX LARYTUBE 9/55

    FDA Adverse Event
    Malfunction ·ATOS MEDICAL AB·Product code KAC·June 29, 2017

    HANAROSTENT ESO TTS FC 20 DM 15CM 230

    FDA Adverse Event
    Injury ·OLYMPUS AMERICA, INC·Product code KAC·December 16, 2022