BEUDAMED
    8 results · 19ms · 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 ×

    DEPUY ORTHOTECH RESTORE ORTHOBIOLOGIC SOFT TISSUE IMPLANT

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

    PROPELLER HEAD

    FDA UDI
    Biomet Orthopedics, LLC·00880304417083·

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111062·INSTRUMENT CASE MEDIUM ALUMINUM

    BARD BAIM-TURI BALLOON DIAGNOSTIC PACING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRIMARY CARE SOLUTIONS, INC., STERILE WATER AND SALINE FOR IRRIGATION

    FDA 510(k)
    FDA Unclassified ·Unknown

    CATHETER

    FDA Adverse Event
    Injury ·I-FLOW, LLC·Product code BSO·February 22, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FNL·January 13, 2011

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·August 5, 2014