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

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    NONIN MEDICAL, INC., MODEL 7500 DIGITAL PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B5820802550·RETRACTOR, ALL TYPES

    COBE SMARXT OPTIMA XP SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CAVITY VARNISH

    FDA 510(k)
    FDA Class 2 ·Dental

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962155752·PEEK, LONGITUDINAL BLUNT BLADE, 19MMX55MM WIDE

    UNIFY QUADRA CRT-D, DF4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·April 26, 2013

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 7, 2011

    RESTORE ADVANCED RECHARGEABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·July 22, 2008

    VORTEK J PERCUTANEOUS NEPHROSTOMY CATHETER

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code LJE·August 30, 2023

    HANDLE CEV102910R DIA 10MM ANG W/RATCHET [MXI/XOM]

    FDA Adverse Event
    Injury ·XOMED MICROFRANCE MFG·Product code GCJ·December 20, 2013