BEUDAMED
    12 results · 27ms · Sources: EU EUDAMED, US FDA

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    STERILE SALINE - FOR SUCTION CATHETER LUBRICATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317358813·

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756235747·LTX-SAFE STND-OTOLARYNGLGY/EAR

    DEKNATEL

    FDA UDI
    TELEFLEX INCORPORATED·04026704421978·CTY GN BR 0 KHT-3 1N 18

    DEKNATEL

    FDA UDI
    TELEFLEX INCORPORATED·14026704716637·CTY GN BR 0 KHT-3 1N 18

    DEKNATEL

    FDA UDI
    TELEFLEX INCORPORATED·34026704421979·CTY GN BR 0 KHT-3 1N 18

    OPERAID DISPOS. IRRIGATING KNIFE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    MEDIFLEX INJECTION CAP

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

    ACCU-CHEK ® INFORM METER

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·June 25, 2014

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 3, 2013

    S-ROM SLEEVE PRX ZTT, 18B-SML

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code MRA·November 5, 2010

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·August 15, 2018