BEUDAMED
    8 results · 18ms · 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.

    MORGAN SUTURE-DRILL

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

    Stainless Steel Wire

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746047411·WIRE SS UPPER 019 X 025 FORM II 10/PK

    Advanced Perfusion System 1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CHUNG CHENG FAR INFRARED RAY HEALTHFUL LAMP (OR MEDICAL FIR RADIATOR), MODEL CH-8810

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·April 7, 2014

    PUMP MMT-722NAS PRDGM INS V2.2 SK EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·October 1, 2010

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON INC·Product code FTL·November 30, 2012

    MICROFIX QA+#3/0 OC V-4W/BIT

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code HTY·January 22, 2019