BEUDAMED
    158 results · 28ms · Sources: EU EUDAMED, US FDA

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    STERILE GC SUPPLEMENT (W/O ANTIBIOTICS)

    FDA 510(k)
    FDA Class 1 ·Microbiology

    AcQMap

    FDA UDI
    ACUTUS MEDICAL, INC.·00857042007357·Workstation Cable

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306809972·Mercedes Cannula, 11G x 25cm, 60cc

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00844856072404·CP Ti STRAIGHT ROD, 5.5mm X 200mm

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00844856072435·CP Ti STRAIGHT ROD, 5.5mm X 500mm

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00844856072428·CP Ti STRAIGHT ROD, 5.5mm X 400mm

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00844856072411·CP Ti STRAIGHT ROD, 5.5mm X 300mm

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00844856072442·CP Ti STRAIGHT ROD, 5.5mm X 600mm

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197494281·Micro Scissors straig...

    COBE SMARXT OPTIMA XP SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NONIN MEDICAL, INC., MODEL 7500 DIGITAL PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962158579·MICRO FRACTURE AWL, W/CARBON FIBRE HANDLE, 25° TIP

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 24, 2025

    USS-VAS Ø6.2 L40 TAN DBLUE

    FDA Adverse Event
    Injury ·SYNTHES MEZZOVICO·Product code NKB·May 8, 2014

    GOBED II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·October 8, 2012

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·August 31, 2007

    Power Processor Aliquot Tube Labels Part 800255

    FDA Recall
    Terminated ·Beckman Coulter Inc·June 23, 2003

    PHYSICA TT

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code MBH·December 21, 2023

    Puritan Bennett 560 Ventilator, PB560, CFN 4096600

    FDA Recall
    Open, Classified ·Covidien Llc·Product code QOS·August 19, 2022

    Puritan Bennett 840 ventilator systems software part number 4-070212-85, revision AB-AG. The intended use of the product is to provide mechanical ventilation to patients.

    FDA Recall
    Terminated ·Covidien·Product code CBK·December 16, 2013