BEUDAMED
    18 results · 24ms · Sources: EU EUDAMED, US FDA

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    Straumann Variobase Abutment NNC, Straumann Variobase Abutment RN, Straumann Variobase Abutment WN, Straumann Variobase Abutment NC, Straumann Variobase Abutment RC, IPS e.max CAD MO Coping, IPS e.max CAD LT Crown, IPS e.max CAD HT Crown, coron CoCr Single Unit

    FDA 510(k)
    FDA Class 2 ·Dental

    Suture Forceps

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896103511·Stern Castroviejo Suture Forceps Straight 1 x 2...

    STERN-CASTROVIEJO SUTURE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896015685·STERN-CASTROVIEJO SUTURE FORCEPS STRAIGHT TIPS ...

    TRIAGE D-DIMER TEST, MODEL 98100

    FDA 510(k)
    FDA Class 2 ·Hematology

    K-SHIELD SMALL VEIN INFUSION / WINGED COLLECTION SET W/ ANTI NEEDLE STICK PROTECTOR (AND MULTISAMPLE LUER ADAPTER)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TRIAGE D-DIMER PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code GHH·May 11, 2018

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·May 7, 2019

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·May 7, 2019

    TRIAGE D-DIMER TEST

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·October 2, 2019

    TRIAGE D-DIMER PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·September 17, 2019

    TRIAGE D-DIMER PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·May 7, 2019

    TRIAGE D-DIMER PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code GHH·August 17, 2018

    INDIGO SYSTEM ASPIRATION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code QEW·August 7, 2023

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 3, 2013

    JUVEDERM ULTRA XC TSK US

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·September 23, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 20, 2011

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·February 22, 2019

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·September 5, 2017