BEUDAMED
    352 results · 26ms · Sources: EU EUDAMED, US FDA

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    ERBE HELIX HYDRO-JET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Baltic Denture System BDLoad

    FDA UDI
    Merz Dental GmbH·D7091033590·Baltic Denture System BDLoad BDLoad Sm7 PLSEbm...

    MAXIM PF MODELS 033-581/033-590

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Gibralt®

    FDA UDI
    INNO Holdings, Inc.·M711050020335900·Posterior Cervical, Rod, Prebent, Ti, 3.5mm x 9...

    Gibralt

    FDA UDI
    Choice Spine, LP·10885862223159·

    GRAMS POLYESTER NONABSORBABLE SUTURE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    POWDERED NATURAL AND/OR COLORED LATEX EXAM GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ALPHATEC

    FDA Adverse Event
    ALPHATEC MFG INC. AKA NEXMED INC·Product code HWC·February 26, 2004

    PDS II (POLYDIOXANONE) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAN·April 3, 2013

    COLLEAGUE CX TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·March 30, 2011

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·April 23, 2008

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

    BD PHOENIX¿ NMIC/ID-307

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

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 9, 2025