BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    BARD SINGULAR BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526799332·MANUMED ACTIVE WRIST LEFT SILVER L

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523154128·Tesera X Angled Trial, 60mm x 22mm x 14mm x 0°

    CRYOPEN AND ACCESSORIES

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

    OCTRODEX(TM), QUATTRODEX(TM), INTRODEX(TM), EPIDURAL NEEDLE, STYLETS

    FDA 510(k)
    FDA Class 2 ·Neurology

    EDGE CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·SUPERDIMENSION INC.·Product code JAK·May 13, 2014

    ASR UNI FEMORAL IMPL SIZE 41

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 11, 2013

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·November 18, 2010

    smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·March 27, 2024

    paraPAC 300 ventilator kit without internal PEEP and CPAP, Item Number P300N

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·October 2, 2024