BEUDAMED
    22 results · 23ms · Sources: EU EUDAMED, US FDA

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    TIGERVIEW PROFESSIONAL

    FDA 510(k)
    FDA Class 2 ·Radiology

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70610351·Mini Sprint-Brackets 5-5 McLaugh/Benn/Trev. .01...

    AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 35mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665020953·

    SENSITITRE 18-24 HOURS SUSCEPTIBILITY PLATES (GATIFLOXACIN)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    DIMENSION DRUG CALIBRATOR, MODEL DC22B

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710610350100·Tri-Channel Met-Traverse, 35mm x 10mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710610350070·Tri-Channel Met-Traverse, 35mm x 7mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710610350090·Tri-Channel Met-Traverse, 35mm x 9mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710610350080·Tri-Channel Met-Traverse, 35mm x 8mm

    RU NOVOSIBIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 16, 2013

    ST JOSEPHS PHOENIX, AZ 1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code DWF·July 31, 2009

    RU NOVOSIBRIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·April 11, 2013

    RU NOVOSIBIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DWF·October 16, 2013

    CP87170 DE MUENCHEN

    FDA Adverse Event
    Death ·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011

    3M ESPE RETRACTION CAPSULE

    FDA Adverse Event
    Malfunction ·3M DEUTSCHLAND GMBH·Product code MVL·April 9, 2013

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·April 8, 2011

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 13, 2008

    CP87641 GB SOUTHAMPTON

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DWE·March 22, 2010

    D 100 PH.I.S.I.O. NEWBORN HOLLOW FIBER MEMBRANE OXYGENATOR WITH RESERVOIR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code DTZ·March 28, 2017

    ENCOREANYWHERE

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·February 17, 2016