BEUDAMED
    37 results · 17ms · Sources: EU EUDAMED, US FDA

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    MODEL M1175A/M1176A WITH ST SEGMENT MONITORING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950022823·SUCTION TIP SCREW TYPE OPENING 2MM 4-1/2" 11.5CM

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746097065·DB BKT MASTER IBD LL CUSP 022 T-11 A+7 R=0

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746094217·DB BRACKET MASTER SERIES MAND RIGHT/LEFT 2ND BI...

    ReWalk P6.0

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    LEVEEN NEEDLE ELECTRODE

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

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·AIS EXIMER LASER ANGIOPLASTY

    SNAP-RING FOR 52MM OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·December 4, 2007

    Iron Intern

    FDA UDI
    Automated Medical Products Corp.·00810118340000·29-00032 Extra Long Articulating Dissector

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·EXCIMER LASER

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·EXCIMER LASER (LASER CATHETER-MODEL PC4021(1.6MM))

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·EXCIMER LASER MODEL DYMER (R) 200+

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·EXCIMER LASER MODEL PC4016(1.3MM),4026(1.6MM)

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·EXCIMER LASER (LASER CATHETER-MODEL PC4010(1.3MM))

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·EXCIMER LASER

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·EXCIMER LASER MODEL LAISER II

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·EXCIMER LASER

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·EXCIMER LASER (LASER CATHETER-MODEL PC4030(2.0MM))

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·EXCIMER LASER MODEL DYMER (R) 200+

    TYPE7B

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·May 27, 2014