BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    IdentiTi Porous Ti Interbody System; IdentiTi NanoTec Interbody System; IdentiTi Cervical Porous Ti Interbody System; IdentiTi NanoTec Cervical Interbody System; IdentiTi Cervical Standalone Interbody System; IdentiTi NanoTec Cervical Standalone Interbody System; IdentiTi ALIF Standalone Interbody System; IdentiTi NanoTec ALIF Standalone Interbody System; Transcend PEEK Interbody System; Transcend NanoTec Interbody System; Transcend Cervical PEEK Interbody System; Transcend NanoTec Cer

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Blazer™ Dx-20 Bidirectional Steerable Diagnostic Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ELIA M2; IMMUNOASSAY, POSITIVE CONTROL 100, POSITIVE CONTROL 250

    FDA 510(k)
    FDA Class 2 ·Immunology

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

    Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control

    FDA classification
    FDA Class 2 ·Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control

    Catheter, Electrode Recording, Or Probe, Electrode Recording

    FDA classification
    FDA Class 2 ·Catheter, Electrode Recording, Or Probe, Electrode Recording