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

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    Medline Cautery Electrode (PTFE)

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

    ACLEARA, THERACLEAR

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

    PREMIUM

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

    MIO ADVANCE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code FPA·July 20, 2021

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 7, 2025

    ELLIPSE DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·October 15, 2014

    REDUC-FORCEPS TOOTHED RATCH-LOCK L140

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTD·June 17, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 24, 2011

    BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQO·January 18, 2019

    BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·November 26, 2019

    BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·November 26, 2025