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

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    PHYSIOFLOW ENDURO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bernafon

    FDA UDI
    Bernafon AG·05711584003459·MD3 CPx, VC PS GB MONDO 3

    HAND SURGERY OSTEOTOME

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896052574·HAND SURGERY OSTEOTOME STRAIGHT BLADE

    SIMPLICITY WITH WINGS INFUSION SET, (MODEL MMT-103)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RELISA PR3-ANCA TEST SYSTEM FOR ANTIBODIES TO PROTEINASE 3, MODEL # 7096-16

    FDA 510(k)
    FDA Class 2 ·Immunology

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·October 24, 2015

    VA LOCKSCR Ø2.4 SELF-TAP L12 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 18, 2013

    VALIANT CAPTIVIA

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·May 9, 2013

    PEEK TENODESIS SCREW, 6.25MM X 15MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·May 26, 2011

    *

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JTC·May 19, 2008

    VA LOCKSCR Ø2.7 HEAD 2.4 SELF-TAP L14 TA

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·April 27, 2022

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·September 16, 2016

    FIAB EURODEFIPADS

    FDA Adverse Event
    Malfunction ·FIAB S.P.A.·Product code LDD·October 19, 2022

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·December 29, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·July 30, 2015

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·December 30, 2014

    UNK - SCREWS: 2.7 MM VA LOCKING

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·March 1, 2024

    EURODEFIPADS

    FDA Adverse Event
    Malfunction ·FIAB SPA·Product code LDD·April 19, 2023

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 22, 2016

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 12, 2016