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.

    LIGHT PATCH

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ARGELOY N.P.

    FDA 510(k)
    FDA Class 2 ·Dental

    ARGILITE 4 GOLD ALLOY FOR PORCELAIN

    FDA 510(k)
    FDA Class 1 ·Dental

    1.5MM MANDIBLE ELEVATED MESH FOOT B-TYPE 5.5MM OFFSET

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MQN·March 7, 2013

    HUDSON SPIRAL-FLEX ET TUBE 7.0

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·January 6, 2011

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014