BEUDAMED
    8 results · 20ms · 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.
    Filters Regulation: Us FDA ×

    BLUEPRINT Patient Specific Instrumentation

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B5821605550·RETRACTOR, ALL TYPES

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528126400·3.0/4.0mm T10 Driver, Cannulated, Long, Quick R...

    SPRAYGENIX CRYO ABLATION SYSTEM

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

    APEX-LNK ACETABULAR INSERT, E, APEX-LNK ACETABULAR INSERT, F, APEX-LNK

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAPSURE SENSE

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    SHILEY LOW PRESSURE CUFFED

    FDA Adverse Event
    Injury ·COVIDIEN / FORMERLY TYCO HEALTHCARE·Product code JOH·July 6, 2011

    CONNECSCR F/DHS/DCS-WRENCH NO. 338.300

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWB·June 10, 2013