BEUDAMED
    29 results · 26ms · Sources: EU EUDAMED, US FDA

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    F5 Corpus VS

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    GE LOGIQ P6/P6 PRO

    FDA 510(k)
    FDA Class 2 ·Radiology

    INOMED ADHESIVE LARYNGEAL ELECTRODES, MODELS 530655, 530656

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    G7 SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PBI·June 2, 2017

    AVAN CMNTD SHELL SS 50MM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·April 24, 2026

    MODULAR CUP SYSTEM, RIMCUP

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    AVAN CMNTD SHELL SS 50MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 21, 2026

    RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM 6

    FDA Adverse Event
    Malfunction ·GUIDANT CARDIAC SURGERY·Product code GEI·October 1, 2008

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KXA·June 26, 2013

    3002 SECURE II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·July 29, 2011

    RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018

    G7 BONEMASTER LTD ACET SHL 58G

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·September 23, 2019

    G7 FINNED BM 3 HOLE SHELL 48C

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·May 16, 2018

    DURAL ALPHA INSERT NEUTR JJ/36

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LZO·February 18, 2026

    G7 BONEMASTER LTD ACET SHL 46B

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·July 18, 2019

    G7 BONEMASTER LTD ACET SHL 52E

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 14, 2018

    G7 BONEMASTER ACETABULAR SHELL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PBI·September 5, 2017