BEUDAMED
    8 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.

    ALTRACLUDE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    AURADONICS

    FDA UDI
    AURADONICS INC.·00810033836800·LATEX ELASTICS 1/8" 6.5 oz. - AMBER, 2000 ea., ...

    TSRH® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00673978042671·CROSSLINK 811-303 LP 5.5MM LEN .875 TI

    RANDOX PHENOBARBITAL

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    DERMATOLOGICAL TREATMENT DEVICE FAMILY

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

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·October 31, 2012

    SC2000

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 11, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·August 11, 2010