BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    MERIFLUOR TM PNEUMOCYSTIS MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Micro ERA® Digital Spacer

    FDA UDI
    STERNGOLD DENTAL LLC·00841549119125·A digital spacer for Micro ERA® implant abutmen...

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515230521·Sheehy Fascia Press, 23x31mm plate, 7 1/2"

    11mm TELEPORT Tissue Retractor

    FDA UDI
    INTERVENTIONAL SPINE, INC·81195401001000·

    ORTHOKROME* ANTITHROMBIN

    FDA 510(k)
    FDA Class 2 ·Hematology

    WILSON-COOK RETRIEVAL & GRASPING FORCEPS

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

    *

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·June 13, 2014

    REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 7

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 9, 2013

    HS HAND CONTROLLED CURVED SHEA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code LFL·February 8, 2008

    ARROW CVC SET: 16 GA X 12" (30 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code FOZ·February 22, 2017