BEUDAMED
    26 results · 25ms · Sources: EU EUDAMED, US FDA

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    Erchonia Zerona 6 headed scanner EZ6

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526768505·GENUMEDI PSS GREEN VI

    HHM

    FDA UDI
    Oticon A/S·05707131288912·H110V2 TI, RITE 312 WL TC HHM

    OSS™ Orthopedic Salvage System

    FDA UDI
    Biomet Orthopedics, LLC·00880304239678·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100127·KRATZ-BARRAQUER SPECULUM RIGHT EYE

    FINN MOD TIBIAL BEARING STD 22

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·September 21, 2017

    Tibial Ultra+ Trial Insert Size 5

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215073923·

    BIO-GIDE RESORBABLE BILAYER MEMBRANE FOR GUIDED TISSUE AND BONE

    FDA 510(k)
    FDA Class 2 ·Dental

    CIRCUFLOW 5100 SEQUENTIAL COMPRESSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 12, 2025

    VENOUS WINDOW NEEDLE GUIDE

    FDA Adverse Event
    VITAL ACCESS CORP.·Product code KNW·March 7, 2013

    ECHELON*FLEX45

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 6, 2011

    8F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL·Product code MGB·September 4, 2008

    MEDTRONIC DUAL CHAMBER TEMPORARY EXTERNAL PACEMAKER 510(K) K150246

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DTE·February 10, 2021

    MOD ARTHRO 0 DEG LCK COLLAR

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HSB·October 28, 2021

    OSS MODULAR PROXIMAL TIBIA

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code KRO·December 20, 2016

    UNKNOWN PALACOS CEMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·April 11, 2023

    ORTHOPEDIC SALVAGE SYSTEM FINN MODULAR PROXIMAL FEMORAL COMPONENT RIGHT 7CM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 11, 2025

    ORTHOPEDIC SALVAGE SYSTEM DIAPHYSEAL SEGMENT 17CM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·June 11, 2025

    ASAHI GLADIUS EX

    FDA Adverse Event
    Malfunction ·ASAHI INTECC CO., LTD.·Product code DQX·September 17, 2025