BEUDAMED
    11 results · 24ms · Sources: EU EUDAMED, US FDA

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    VOLUSON I/E

    FDA 510(k)
    FDA Class 2 ·Radiology

    Bernafon

    FDA UDI
    Bernafon AG·05711584050286·PC7 CPX, VC PS BE PRECISO 7

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR31319371·Palatal bar headgear retention size 02 width 37

    HYBRID TROCAR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ALANTECH GRAFT FIXATION SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SEALING UNIT FROM 5MM TROCARS

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GCJ·June 17, 2015

    REDUCING CONVERTER 10/12MM TO 5MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GCJ·June 17, 2015

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·May 29, 2013

    INSYNC SENTRY

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NIK·June 16, 2011

    ACCU-CHEK TENDER INFUSION SET

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code FOZ·August 22, 2008

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Injury ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 2, 2026