BEUDAMED
    10 results · 24ms · 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.

    PLAIN/CHROMIC CATGUT

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

    NANOHYBRID COMPULES 15-.3 Gm (A2)

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77819940021·Nanohybrid Composite contains a new ytterbium f...

    ORTHOFIX GALAXY FIXATION SYSTEM

    FDA UDI
    ORTHOFIX SRL·18052469471111·GALAXY FIXATION GEMINI ANKLE 4MM KIT MULTISCREW...

    CYTOMEGALOVIRUS FLUORESCENT MONOCLONAL ANTIBODY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FLEXIBLE BRONCHOSCOPE

    FDA Adverse Event
    Death ·OLYMPUS·Product code EOQ·September 16, 1994

    RUSCH ENDOTRACHEAL TUBE WITH CUFF

    FDA Adverse Event
    Death ·RUSCH·Product code LNZ·September 16, 1994

    QUADCUT STRAIGHTSHOT

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC·Product code HTT·March 1, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 16, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·August 8, 2014