BEUDAMED
    6,328 results · 28ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO TSRH SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·January 27, 2012

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code MNI·April 16, 2013

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040013083·Zirlux 16+ C2 98.5X10

    ROLLO 110X20X16E/QT-HS/MINDRAY D60

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763087830·

    DMI

    FDA UDI
    D-M-S HOLDINGS, INC.·00041298001676·Lightweight Extra-Wide Aluminum Rollator

    FOSTER GRANT

    FDA UDI
    FGX INTERNATIONAL INC.·00193033316917·

    FOSTER GRANT

    FDA UDI
    FGX INTERNATIONAL INC.·00193033316924·

    DMI

    FDA UDI
    D-M-S HOLDINGS, INC.·00041298001690·ROLLATOR ALUM 8 IN WHEELS

    STILLE Scissors

    FDA UDI
    Stille AB·07332339101848·STILLE NASAL SCISSORS SuperCut angled 18 cm 7 in

    FOSTER GRANT

    FDA UDI
    FGX INTERNATIONAL INC.·00193033316894·

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07310K0100290·Caddie Lid, MIS Rods and Caps

    HOME HEALTH MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GEIGER NEEDLE ADAPTER, MODEL 406

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

    INTERFACE RESPONSE 2.0 INCREMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·March 14, 2013

    ENDOSCOPIC BILIARY CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code LQR·March 8, 2011

    TENDRIL DX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2008

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·April 23, 2021

    IMPL TAPERED SCR-V SBM 3. 7MM 3.5MM 8MM

    FDA Adverse Event
    Malfunction ·ZIMMER DENTAL·Product code DZE·December 19, 2019

    IMPL TAPERED SCR-V HA 3.7 MM 3.5MM 13MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·August 7, 2019