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

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    ABR-2000

    FDA 510(k)
    FDA Class 2 ·Neurology

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040016831·CHANNELS MTA RC SEALER    EA

    Prep&Etch™

    FDA UDI
    SAFCO DENTAL SUPPLY CO.·D72310203603·Safco 38% phosphoric acid for etching dentin, e...

    GALILEO® TROCHANTERIC NAIL, LEFT, Ø10mm x 36cm x 125°

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665021943·

    Midway Everyday

    FDA UDI
    MIDWAY DENTAL SUPPLY, LLC·10843717103469·Midway Everyday Autoclave Pouches 3 1/2 x 9 (200)

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450157206·

    CLOUD CUFF

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RX G-UNIVERSAL

    FDA 510(k)
    FDA Class 2 ·Dental

    1282497-2001-00002

    FDA Adverse Event
    Injury ·KENDALL CORP·Product code KNT·February 1, 2001

    SOFTCLIX ® LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·March 26, 2013

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·March 11, 2011

    SPIDERFX EMBOLIC PROTECTION DEVICE

    FDA Adverse Event
    Injury ·EV3 INC.·Product code NTE·March 27, 2008

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·February 23, 2024

    PRINEO SKIN CLOSURE SYSTEM UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OMD·February 23, 2024