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

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    Invacare Platinum Mobile Oxygen Concentrator

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    KENSTONE METAL·Product code ITJ·July 20, 2012

    G-FORCE PEEK SUTURE ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REFLECTION 3-HOLE SHELL WITH ASYMMETRIC POROUS COATING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PHILIPS SONICARE

    FDA Adverse Event
    Injury ·Product code EFS·January 25, 2018

    Widex

    FDA UDI
    Widex A/S·05706069975260·WIDEX MOMENT M-CIC-M (TR) 330 (Clay brown)

    Widex

    FDA UDI
    Widex A/S·05706069563535·Widex UNIQUE U-CIC-M TR (Clay brown ) 330, Tran...

    Widex

    FDA UDI
    Widex A/S·05706069563528·Widex UNIQUE U-CIC-M TR (Light beige ) 330, Tra...

    Widex

    FDA UDI
    Widex A/S·05706069563542·Widex UNIQUE U-CIC-M TR (Dark brown ) 330, Tran...

    Widex

    FDA UDI
    Widex A/S·05706069975277·WIDEX MOMENT M-CIC-M (TR) 330 (Dark brown)

    Widex

    FDA UDI
    Widex A/S·05706069975253·WIDEX MOMENT M-CIC-M (TR) 330 (Light beige)

    OXF ANAT BRG LT MD SIZE 4 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 29, 2017

    OXF UNI TIB TRAY SZ AA LM PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 29, 2017

    ST104 TRANSPORT OBS

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·June 30, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·June 10, 2013

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code FZP·September 5, 2008

    CONTOUR® PLUS

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·February 20, 2025

    ALERE DETERMINE HIV 1/2 AG/AB COMBO

    FDA Adverse Event
    Malfunction ·ALERE SCARBOROUGH INC.·Product code MZF·May 24, 2018

    ALERE DETERMINE HIV 1/2 AG/AB COMBO

    FDA Adverse Event
    Malfunction ·ALERE SCARBOROUGH INC.·Product code MZF·May 24, 2018

    ALERE DETERMINE HIV 1/2 AG/AB COMBO

    FDA Adverse Event
    Malfunction ·ALERE SCARBOROUGH INC.·Product code MZF·May 24, 2018