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

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    COMPLETE BRAND COMFORTPLUS MULTI-PURPOSE SOLUTION

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00816577024253·Dynamic Zimmer TSV 3.5mm Non-Engaging Titanium ...

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014602967·Disposable Face Masks

    ORTHO ARCH

    FDA UDI
    Ortho Arch Company Inc·D90980001641·MICRO LIGATURE CUTTER – CURVED ***DISCONTINUED/...

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014600178·SHOULDER CHAIR DISPOSABLE FACE MASK 12/CS

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014602981·Disposable Face Masks (Steris)

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014602998·Disposable Face Masks (Trumpf)

    GOLF BALL TITANIUM TYING FORCEP STR 5MM DELICATE

    FDA UDI
    DAUD JEE MFG. CO·G006DT5070001640·This instrument is used to grasp, retract, or s...

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014602974·Disposable Face Masks (Skytron)

    RS-4M+MUSCLE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SENSATION -VACUUM ASSIST DEVICES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014603001·Disposable Face Masks (Trump Int)

    EUFLEXXA

    FDA Adverse Event
    Injury ·BIO-TECHNOLOGY GENERAL (ISRAEL) LTD·Product code MOZ·July 13, 2017

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·May 24, 2021

    CARDIOSAVE HYBRID, TYPE B PLUG

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

    MERIT CUSTOM KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code FMF·March 8, 2013

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP 2M8063,

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 24, 2011

    CARPENTIER-EDWARDS PERIMOUNT MAGNA AORTIC BIOPROSTHESIS

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code LWR·February 18, 2008

    MYNXGRIP VASCULAR CLOSURE DEVICE 6F/7F

    FDA Adverse Event
    Malfunction ·ACCESSCLOSURE, INC.·Product code MGB·November 14, 2014

    ATELLICA IM HIGH-SENSITIVITY TROPONIN I (TNIH)

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·June 1, 2022