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

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    NITRILE PATIENT EXAMINATION GLOVE POWDER FREE, NON STERILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TruForm

    FDA UDI
    Rmo, Inc.·00885797099815·MX 1-2 BI BD KT N/L UNIV 131

    Ponsky-Gauderer Silicone PEG Tray

    FDA UDI
    Bard Access Systems, Inc.·00801741080906·Ponsky-Gauderer Silicone PEG Kit 20F

    Spacelabs Healthcare

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522125317·LC12 PATIENT CABLE US DEFIB PROTECTED US,ROHS

    SPACELABS HEALTHCARE

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522111884·LC12 PATIENT CABLE US DEFIB PROTECTED US,ROHS

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555159000329·8.2mm Caddy Block

    Disposable Sensor

    FDA UDI
    Honeywell Healthcare Solutions GmbH·04036616007184·Disposable Sensor DI-2221-5 OEM BCI

    STELA UT46 AND BT45/46 STRAIGHT TINED PACING LEADS, STELA UJ45 AND BJ44/45 J-SHAPED TINED PACING LEADS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    VIDEOLABS MEDCAM PROPLUS VIDEO CAMERA AND INTEGRAL LIGHT SOURCE

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

    SURE-T PARADIGM

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

    SOFTPORT DELIVERY DEVICE

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code MSS·December 18, 2014

    SURGISTOOL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FZM·March 12, 2013

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·February 18, 2011

    ICY HOT HEAT THERAPY

    FDA Adverse Event
    Malfunction ·CHATTEM·Product code IMD·February 18, 2008

    DATASCOPE'S 8FR. POLYMIDE 25CC,34CC AND 40CC IAB AND ACCESSORIES, MODELS 0684-00-0327, 06844-00-0328, 0684-00-0329

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AMPLATZER MULTI-FENESTRATED SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MLV·March 13, 2009

    AMPLATZER PFO OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MLV·March 13, 2009

    AMPLATZER SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MLV·March 13, 2009

    AMPLATZER PFO OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MLV·March 13, 2009

    AMPLATZER MULTI-FENESTRATED SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MLV·March 13, 2009