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

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    CORIN OPTIMOM MODULAR HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IMMUKNOW-THE CYLEX IMMUNE CELLFUNCTION ASSAY

    FDA 510(k)
    FDA Class 2 ·Hematology

    SUCTION PUMP FOR INTRACORPOREAL ULTRASOUND LITHOTRIPTER AND ACCESSORIES, MODEL 2207.XXX

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    JRNY BCS PAT RESRF RD 35 MM STD

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·August 30, 2017

    HAHN TAPERED IMPLANT Ø4.3 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·December 4, 2025

    HAHN TAPERED IMPLANT Ø4.3 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·July 20, 2023

    HAHN TAPERED IMPLANT Ø4.3 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·December 5, 2025

    HAHN TAPERED IMPLANT Ø4.3 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·May 26, 2023

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code NRA·October 23, 2017

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code NRA·October 23, 2017

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code NRA·October 23, 2017

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code NRA·October 23, 2017

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code NRA·October 23, 2017

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code NRA·October 23, 2017

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 7, 2013

    SPEEDBAND SUPERVIEW SUPER 7, MODELS 4203

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code MND·June 2, 2011

    SPYGLASS DIRECT VISUALIZATION PROBE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KOG·August 12, 2008

    JOURNEY POLY TIBIAL INSERT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·June 12, 2017

    PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 15, 2025

    HAHN TAPERED IMPLANT Ø4.3 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·June 3, 2022