BEUDAMED
    22 results · 20ms · Sources: EU EUDAMED, US FDA

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    BD AUTOSHIELD DUO PEN NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD INSULIN PEN NEEDLE

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·November 9, 2015

    2.5mm Hex Driver Fixed 300mm

    FDA UDI
    Osteocentric Technologies, Inc.·00816950028595·2.5mm Hex Driver Fixed 300mm

    STARLED5 NX

    FDA UDI
    ACEM SPA·08050705890507·STARLED5 NX TROLLEY

    OTS PG&E Field Kit

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588107035·OTS PG&E Field Kit

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989028492·SS BROAD ARCH LO SML 0180X0250 PK/10

    4WEB Medical

    FDA UDI
    4web Medical·00812998046751·

    Biliary Drainage Tube

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170046582·

    BD IAG BC PRO GLOBAL BLU 22GA X 1.0IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·July 30, 2024

    BD IAG BC PRO GLOBAL BLU 22GA X 1.0IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·July 30, 2024

    INTER-VIAL

    FDA 510(k)
    FDA Class 2 ·General Hospital

    STATIONARY X-RAY SYSTEM (DETECTOR) MODEL: ALTAS

    FDA 510(k)
    FDA Class 2 ·Radiology

    STRATUS CS

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code DAP·November 11, 2015

    STRATUS CS

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code DAP·November 9, 2015

    PENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 10, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 1, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 14, 2008

    Microdot Xtra blood glucose test strips

    FDA Enforcement
    Class II ·Ongoing·Cambridge Sensors Limited·August 28, 2019

    BD IAG BC PRO GLOBAL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 18, 2024

    Ultra-soft SV Monorail Balloon Dilatation Catheters, 4.5 mm/ 2.0 cm/150 cm, Reference Catalog Number 37916-4520

    FDA Recall
    Terminated ·Product code GBR·July 1, 2003