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

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    AssureTech DOA Dipstick Screen Panel Tests, AssureTech DOA Integrated Cup Tests

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116023462·THULIO LL-R TM 270µM 3M SLIM PERF. 3ST 10X USE

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116023264·200 Micron SU Thulio High Performance 3m Fiber

    Dornier Thulio Performance Fiber

    FDA UDI
    INNOVAQUARTZ LLC·00816959021870·

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613154546633·BONE REDUCTION FORCEPS

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981246976·No-Profile Interbody, 31mm x 24mm x 16mm, 30 Deg

    Zodiac

    FDA UDI
    ALPHATEC SPINE, INC.·00844856063136·TI ILIAC BONE SCREW ASSY, 7.5MM X 30MM X 30°

    Zodiac

    FDA UDI
    ALPHATEC SPINE, INC.·00844856063129·TI ILIAC BONE SCREW ASSY, 7.5MM X 30MM X 15°

    BOSTON SCIENTIFIC EXPRESS BILIARY LD PREMOUNTED STENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    KSEA BIPOLAR COAGULATING ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Neurology

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 27, 2014

    ENRHYTHM DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·August 11, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013

    UNKNOWN T2 ALPHA TIBIA NAIL

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HSB·October 15, 2025

    UNKNOWN T2 ALPHA TIBIA NAIL

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HSB·October 15, 2025

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·April 25, 2016

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·April 25, 2016

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·June 27, 2018

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·June 27, 2018

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·November 18, 2019