BEUDAMED
    15 results · 25ms · Sources: EU EUDAMED, US FDA

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    S.E.A.L. FRACTURE FUSION TUBE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981193799·Interbody, 11mm x 40mm x 15mm, 8 deg

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981201784·Interbody, 11mm x 40mm x 15mm, 8 deg

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319704660·Rochester Ochsner (Kocher) Forceps 12" (30cm), ...

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981208905·Trial, 11mm x 40mm x 15mm, 8 deg

    ILLUMINATING SINUS SEEKER

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    MFCD 2320

    FDA 510(k)
    FDA Class 2 ·Radiology

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·June 23, 2014

    K-WIRE

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HWC·December 9, 2016

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·May 25, 2014

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·May 21, 2014

    ZEPHYR XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CRMD·Product code LWP·January 13, 2014

    MAXISKY 440

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH MAGOG INC.·Product code FNG·May 24, 2013

    SYNCHRON® SYSTEMS RHEUMATOID FACTOR (RF) REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·June 25, 2011

    BD VACUTAINER SST BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 12, 2020