BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    Babylog VN800, Babylog VN600

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HEALIX PEEK ORTHOCORD

    FDA UDI
    Medos International Sàrl·10886705007554·HEALIX PEEK 3 - Suture Anchor w/ORTHOCORD PEEK ...

    Steerable IBD

    FDA UDI
    Seaspine Orthopedics Corporation·10889981117290·Fixed Rasp; 22x7 (05-3307)

    Materialise PKA Guide System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AXYA MODEL 3000 AXYALOOP TITANIUM BONE ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TITANIUM HEXED UNISCREW

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code NHA·April 9, 2019

    ENTRALITE INFINITY ENTERAL FEEDING PUMP

    FDA Adverse Event
    Injury ·ZEVEX INC·Product code LZH·November 5, 2008

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 24, 2011

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 12, 2013

    TEMA ELBOW SYSTEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code JDB·September 26, 2024

    5.5 HEALIX3 PEEK ANC.W/OCORD

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·January 29, 2019

    5.5 HEALIX3 PEEK ANC.W/OCORD

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·January 17, 2019

    5.5MM HEALIX PEEK 3-SUTURE ANCHOR W/ORTHOCORD

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·September 7, 2018