BEUDAMED
    11 results · 20ms · 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.

    VIRTUOSO SYSTEM FOR IHC KI-67 (30-9)

    FDA 510(k)
    FDA Class 2 ·Hematology

    cellfina™ system

    FDA UDI
    Merit Medical Systems, Inc.·00884450411070·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197519649·Mayo-Harrington Scissors SuperCut curved...

    STIMUPLEX-DIG-RC NERVE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ENSEAL G2 TISSUS SEALERS

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

    KIT RSV 30 TEST HOSPITAL VERITOR

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 15, 2021

    V.A.C. FREEDOM THERAPY SYSTEM

    FDA Adverse Event
    Injury ·KINETIC CONCEPTS, INC.·Product code OMP·February 15, 2021

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

    EON RECHARGEABLE IPG, 16-CHANNEL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 9, 2011

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·August 14, 2008

    BD VACUTAINER SERUM BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·March 16, 2021