BEUDAMED
    8 results · 34ms · Sources: EU EUDAMED, US FDA

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    ADIDYNE 3000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TYGON PAC-MONITORING LINES & FLUID ADMIN

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GA-B, GA-C, GA-E, GA-I, GA-S, GA-W3A, GA-F3A, GA-IL, GA-SL, GA-W3B, GA-F1A

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

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·April 24, 2014

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    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRX·August 29, 2012

    STERLING ES PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LIT·July 28, 2010

    9MM/130 DEG TI CANN TFNA 235MM/RIGHT - STERILE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HSB·December 1, 2020

    Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010; CD3281-40Q/100056770; CD3297-40/100056933

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018