BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    HEMASORB Resorbable Hemostatic Bone Putty

    FDA 510(k)
    FDA Unclassified ·Unknown

    CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE

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

    NEOPLANT IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    STEM: AMISTEM H HA COATED STD STEM SIZE 1

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·April 25, 2019

    RESERVOIR 1.8ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·October 5, 2014

    DRILL BIT Ø2/1.15 CANN L150/48 3FLUTE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·June 3, 2013

    U-CLIP VALVE CLIP

    FDA Adverse Event
    Injury ·MEDTRONIC PERFUSION SYSTEMS·Product code FZP·June 20, 2011

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 25, 2014