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.
    Filters Regulation: Us FDA ×

    TOTAL SHOULDER PROSTHESIS POLYETHYLENE GLENOIND CO

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LactoScrew

    FDA UDI
    Biomet Orthopedics, LLC·00880304453395·

    EMIT(R) II BARBITURATE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    PROPHY PASTE

    FDA 510(k)
    FDA Class 1 ·Dental

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 28, 2014

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·January 9, 2013

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·November 23, 2010

    REF 905580, 6. 8 mm Lactoscrew 2#2 MBNo. (Lactosorb L-15 resorbable copolymer ) Sterile, EO; Biomet Sports Medicine, Warsaw, IN Product Usage: The Biomet Sports Medicine Soft Tissue Anchoring Devices are resorbable repair devices used to attach soft tissue to bone.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code HWC·January 25, 2012