BEUDAMED
    15 results · 28ms · 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.
    Filters Regulation: Us FDA ×

    ADVANTAGESIM MD WITH CT ATLAS-BASED CONTOURING AND RE-PLANNING OPTIONS

    FDA 510(k)
    FDA Class 2 ·Radiology

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017705·K-Wire, Double Ended, Trocar Point, Diameter Si...

    NexxZr™ T / D-100-10-NT-A400-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271112552·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741320450·

    ihcDirect® WT1 Ab Conjugate 15mL

    FDA UDI
    NOVODIAX, INC.·00850030934925·Clone R1012

    ihcDirect® WT1 Ab Conjugate 5mL

    FDA UDI
    NOVODIAX, INC.·00850030934918·Clone R1012

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674132045060·

    8 CHANNEL CARDIAC PHASED ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    DIMENSION VISA HBA1C, MODEL K3105A

    FDA 510(k)
    FDA Class 2 ·Hematology

    SET, ADMINISTRATION, INTRAVASCULAR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 6, 2016

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 4, 2024

    STOPCOCK MANIFOLD GANGS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FMG·June 17, 2020

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    AMPLATZER® SEPTAL OCCLUDER

    FDA Adverse Event
    AGA MEDICAL CORPORATION·Product code MLV·June 16, 2011

    PCA MTK PATELLAR MEDIUM OBSOLETE PRODUCT NO

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code HTG·August 21, 2008