BEUDAMED
    408 results · 22ms · Sources: EU EUDAMED, US FDA

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    HEARTNAVIGATOR RELEASE 2.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    BENCO

    FDA UDI
    BENCO DENTAL SUPPLY CO.·00366975002532·Tubing with Indicator 6" x 100'

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981201708·Interbody, 11mm x 40mm x 13mm, 8 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981193713·Interbody, 11mm x 40mm x 13mm, 8 deg

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319704578·Rochester (Pean) Hemostatic Forceps 6-1/4" (15....

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981208820·Trial, 11mm x 40mm x 13mm, 8 deg

    Restore

    FDA UDI
    KEYSTONE DENTAL, INC.·D768L14013802K0·Drill

    Restore

    FDA UDI
    KEYSTONE DENTAL, INC.·D768L14013801K0·Drill

    ZODIAC POLYAXIAL SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VICEROY INFLATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PFNA-II BLADE L85 TAN

    FDA Adverse Event
    Injury ·SYNTHES BETTLACH·Product code HSB·October 3, 2014

    OPEN PIVOT MECHANICAL HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC ATS MEDICAL·Product code LWQ·May 31, 2013

    SYNCHRON LX RHEUMATOID FACTOR (RF) REAGENT

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

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 19, 2025

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code NJR·April 17, 2026

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 14, 2026

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026