BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    HEMOCLIP SURGICAL OCCLUDING CLIP

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

    Leica Biosystems

    FDA UDI
    Leica Biosystems Richmond, Inc.·20849832024808·Apex PT Control Box Slides, Pink

    NovaPort cannula

    FDA UDI
    novalung GmbH·04260058550742·The NovaPort® one cannulas are thin-walled, wir...

    BaseVac

    FDA UDI
    R. E. Morrison Equipment Inc·D13028000790·3SUR4.40-2-3P | 3P 22 User Triple Surgical Vacu...

    S8 ESCAPE II

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M

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

    SMR REVERSE HUMERAL BODY

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·October 21, 2022

    AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FSA·May 8, 2014

    PEAK PULSAR GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 17, 2012

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·August 11, 2010

    SMR REVERSE HUMERAL BODY

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·October 21, 2022

    Model: CT 5300; Product Code (REF): 728285; Software Versions: 5.1.0.X & 5.1.1.X;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS·November 5, 2025