BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Medline ReNewal Reprocessed Carter-Thomason Needle Point Suture Passer

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

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A182828150·18mm H x 28mm W x 28mm L x 15 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A182828120·18mm H x 28mm W x 28mm L x 12 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A18282880·18mm H x 28mm W x 28mm L x 8 degrees ALIF

    REVIVE INTERMEDIATE CATHETER (REVIVE IC)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SUTURTEK 360 DEGREE STERNAL CLOSURE DEVICE

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

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 17, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 11, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·July 28, 2011

    SKINTACT

    FDA Adverse Event
    Injury ·LEONHARD LANG GMBH·Product code GEI·January 25, 2022