BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    Dynamic TiBase

    FDA 510(k)
    FDA Class 2 ·Dental

    NA

    FDA UDI
    Synthes GmbH·10886982151827·3.5MM LOCKING SCREW SLF-TPNG W/STARDRIVE(TM) RE...

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112779·BARRON VACUUM PUNCH 8.0MM

    Nex-Link®

    FDA UDI
    ZIMMER SPINE, INC.·00889024332676·

    Origin Size 8 Template

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215074715·

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX¿ SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·August 5, 2021

    ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDPOR COATED TEAR DRAIN

    FDA 510(k)
    FDA Unclassified ·Unknown

    PROCEED MULTI-LAYER LAMINATE MESH

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·October 24, 2008

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 15, 2011

    COULTER® LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 8, 2013