BEUDAMED
    10,000 results · 122ms · Sources: EU EUDAMED, US FDA

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    OOFS Pace XL Stimulator

    FDA UDI
    AXIOBIONICS·B36712159L00·Neuromuscular Stimulator

    NAVITOR VISION

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NPT·April 3, 2025

    SABRASET 500100

    FDA Adverse Event
    Malfunction ·SABRATEK CORP.·Product code FPA·June 20, 1997

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·June 6, 2014

    MCGHAN

    FDA Adverse Event
    MCGHAN MEDICAL CORP·Product code FWM·January 24, 2005

    MCGHAN

    FDA Adverse Event
    MCGHAN MEDICAL CORP·Product code FWM·January 31, 2005

    NAIL HANDLE

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code MDM·June 23, 2005

    TERUMO

    FDA Adverse Event
    Injury ·TERUMO CORPORATION·Product code FJI·December 18, 1993

    HEPARIN 1000 U/ML

    FDA Adverse Event
    Injury ·BAXTER·Product code NZW·January 30, 2008

    ALLERGAN BIOCELL TEXTURED IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN·Product code FWM·July 5, 2019

    SWANSON TITANIUM BASAL THUMB

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KYI·November 4, 1997

    HEPARIN 1000 U/ML

    FDA Adverse Event
    Injury ·BAXTER·Product code NZW·January 30, 2008

    PASSIVE PLUS

    FDA Adverse Event
    Injury ·PACESETTER INC.·Product code DTB·February 6, 1998

    SYNCHRONY II

    FDA Adverse Event
    Injury ·PACESETTER INC.·Product code DXY·February 6, 1998

    ACTIVE FIXATION ENDOCARDIAL LEAD

    FDA Adverse Event
    Injury ·PACESETTER INC.·Product code DTB·February 6, 1998

    CHOLANGIOGRAM CLAMP RATCHET, 5MM 32CM

    FDA Adverse Event
    Malfunction ·KOSCHER & WUERTZ GMBH / CHIRURGISCHE INSTRUMENTE·Product code KOG·February 15, 2007

    PARAGON III

    FDA Adverse Event
    Injury ·PACESETTER INC.·Product code DXY·February 6, 1998

    STAGE IV

    FDA Adverse Event
    Malfunction ·SENTECH·Product code FNL·September 18, 2009

    HEARTMATE II

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·March 28, 2013

    G2 FILTER SYSTEM, FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·February 27, 2006