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

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    APN-2 USA SERIES FLEXIBLE CHOLEDOCHOSCOPE

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

    RIWOtrack Clipsensor

    FDA UDI
    Fiagon GmbH·04260759930102·Navigation probe, component of RIWOtrack Naviga...

    FOSTER GRANT

    FDA UDI
    FGX INTERNATIONAL INC.·00193033444931·

    ISLAND WOUND DRESSING WITH MICROBAN

    FDA 510(k)
    FDA Unclassified ·Unknown

    MAGELLAN VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    0009613348-2024-012951

    FDA Adverse Event
    Injury ·INSTITUT STRAUMANN AG·Product code DZE·September 30, 2024

    POSSIS SUTURELESS MYOCARDIAL LEAD

    FDA Adverse Event
    Injury ·POSSIS MEDICAL, INC.·Product code LWS·November 21, 1995

    AMI

    FDA Adverse Event
    Other ·AIRWAY MANAGEMENT INC.·Product code LRK·July 10, 2013

    Z.S.G.M. CUTTER 1.5:1 RATIO ( CAUTION: SHARP )

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·January 25, 2024

    11.0 CM LONG ATTACHMENT

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·March 1, 2013

    TRIATHLON-CR FEMORAL COMPONENT CEMENTED #5 RIGHT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS LIMERICK·Product code JWH·March 2, 2011

    CHARITE ARTIFICIAL DISC, SIZE UNK

    FDA Adverse Event
    Injury ·DEPUY SPINE, INC.·Product code MJO·March 13, 2008

    PENUMBRA SYSTEM JET7 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·August 27, 2020

    DISC HUM 4X100MM RT FLANGED C

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDC·August 15, 2012

    DISC CONDYLE KIT W/ HEXALOBULA

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDC·August 15, 2012

    DISC ULNA 4X75MM RT W/BRNG C

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWT·August 15, 2012

    3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 5 X 10MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·July 16, 2021

    FLEXCATH ADVANCE STEERABLE SHEATH

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DRA·January 14, 2020

    ACHIEVE MAPPING CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DRF·January 14, 2020

    UNKNOWN RIGIDFIX CROSS PIN

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code MAI·July 1, 2019