BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    PERFUSION MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Convaid

    FDA UDI
    CONVAID PRODUCTS, INC.·00840117408340·

    EZ Rider

    FDA UDI
    CONVAID PRODUCTS, INC.·10840117400068·EZ Rider models are manual wheelchairs intended...

    Convaid

    FDA UDI
    CONVAID PRODUCTS, INC.·10840117400686·

    Apple-Hunt Secondary Cannula

    FDA UDI
    Coopersurgical, Inc.·00888937004007·Apple-Hunt Secondary Cannula™ Pyramidal Tip; 10...

    FUTURA SAFETY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HANAROSTENT Esophagus TTS (CCC), HANAROSTENT Esophagus TTS (NCN)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·June 27, 2014

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·January 8, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 17, 2010

    BIOMET StageOne Knee Tibial Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 433165.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020