BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    ELECTRONIC LAPAROFLATOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122376·K-WIRE - SINGLE TROCAR THREADED 1.6mm DIA x 230mm

    Gammex PI Hybrid Surgical Gloves

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    CLICKZIP NEEDLE RETRACTABLE SAFETY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TT (TRACHEOSTOMY TUBES)

    FDA Adverse Event
    Malfunction ·Product code BTR·October 24, 2017

    TI COLLAR WITH GROOVES

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MNI·June 5, 2012

    REVEAL DX

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO, JUNCOS·Product code DSI·February 9, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 6, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014