BEUDAMED
    10 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.

    CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517379580·16 x 11 x 25mm - 5 deg CoRoent LW-L Asse

    Arch Lock

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746146756·ARCH STOP WELDABLE 1.25MM 021X028 100/PKG

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209104956·KIT, TRAUMA LIFE SAVER - COY - 3 SOUTH

    TiTHON Staple with OsseoTi Technology

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TITAN OTR NAR SCRO 18CM

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FHW·June 22, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 5, 2014

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NVY·June 17, 2015

    PUMP MMT-722NAB PRDGM INS V2.2 BL EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·September 28, 2010