BEUDAMED
    7 results · 29ms · Sources: EU EUDAMED, US FDA

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    KARL STORZ FRIMBERGER VARIOGUIDE

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

    DIVERGENCE-L ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SILVER SHIELD ANTIMICROBIAL SKIN AND WOUND GEL, MODEL 3015-S

    FDA 510(k)
    FDA Unclassified ·Unknown

    PINN CAN BONE SCREW 6.5MMX20MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NDJ·February 14, 2013

    MEDISENSE OPTIUM

    FDA Adverse Event
    Malfunction ·Product code NBW·January 17, 2011

    COULTER ACT DIFF ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 28, 2014

    Medtronic INTREPID Spinal System SPACER M 37X27, 12 DEG, Size: 10MM, Part Number: REF 7962210; 12MM, REF 7962212; 14MM, REF 7962214; 16MM, REF 7962216; 18MM, REF 7962218; 20MM, REF 7962220; USA, Rx only, STERILE R. The INTREPID Spinal System is indicated for use with autogenous bone graft in patients with degenerative disc disease.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code MAX·February 6, 2009