BEUDAMED
    21 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    REHCOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040037116·Instant Summer Hot

    MULTECON BLOOD GAS CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CrossBay Cervical Dilator Catheter System

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATIA)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code KNW·June 7, 2006

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556811146·HUMERAL HEAD TRL 50X18 CONCENTRIC

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556811153·HUMERAL HEAD TRL 50X21 CONCENTRIC

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556811108·HUMERAL HEAD TRL 44X16 CONCENTRIC

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556811115·HUMERAL HEAD TRL 44X18 CONCENTRIC

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556811177·HUMERAL HEAD TRL 53X22 CONCENTRIC

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556811085·HUMERAL HEAD TRL 41X15 CONCENTRIC

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556811122·HUMERAL HEAD TRL 47X16 CONCENTRIC

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556811078·HUMERAL HEAD TRIAL 38X14 CONCENTRIC

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556811139·HUMERAL HEAD TRL 47X18 CONCENTRIC

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556811160·HUMERAL HEAD TRL 53X19 CONCENTRIC

    NV GXL LINR, NTRL, 36MM ID, GROUP 4 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·August 26, 2024

    COBAS E411 RACK SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·March 5, 2013

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 8, 2011