BEUDAMED
    6 results · 17ms · 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.

    MARCO STANDARD LENSMETERS 101,201

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    FALLER STYLET

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

    SYDNEY IVF BLASTOCYST CRYOPRESERVATION KIT AND SYDNEY IVF BLASTOCYST THAW KIT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    55 CM 5 FR. D/L GROSHONG NXT UPFT WITH MI AND TLS

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code LJS·November 18, 2010

    NEXGEN LPS-FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code JWH·January 23, 2013

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 11, 2014