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

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    DORO HEADREST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Scanlan® SURG-I-BAND® color coding

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159001631·Scanlan® SURG-I-BAND® color coding - Labels-Sol...

    Battalion

    FDA UDI
    ALPHATEC SPINE, INC.·00840967188331·Battalion, LLIF Trial, 0°, 18 mm Wide, 08 mm X ...

    Battalion

    FDA UDI
    ALPHATEC SPINE, INC.·00190376004297·BATTALION, LLIF PRIMARY DISTRACTOR, 1/4" SQ. ST...

    RICH-MAR WINNER ST4 MUSCLE STIMULATOR, INTERFERENTIAL, AND TENS DEVICE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TEMPTELLER INFRARED EAR THERMOMETER, MODELS TT-901, TT-911 AND TT-921

    FDA 510(k)
    FDA Class 2 ·General Hospital

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00811801036330·18x45 Distractor Rasp – 8mm

    General Instrument

    FDA UDI
    ALPHATEC SPINE, INC.·00840180509982·LLIF DISTRACTOR PARTIAL RASP, 1/4" SQ., 18MM X ...

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180501368·18x45 Distractor Rasp – 8mm

    Intervertebral Disc Preparation Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00190376381145·LIF, BROACH, CC OFFSET, 18MM X 08MM

    Intervertebral Disc Preparation Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00190376380759·LIF, BROACH, STRAIGHT, 18MM X 08MM

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00811801036378·18x45 Distractor Rasp – 8mm, Offset

    Valence Robotic Navigation System

    FDA UDI
    ALPHATEC SPINE, INC.·00190376647104·BROACH, LIF NAV, STRAIGHT, 18MM X 08MM

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·November 5, 2024

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·July 16, 2024

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·August 30, 2023

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·February 7, 2025

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·April 12, 2024

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·February 21, 2024

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 27, 2025