BEUDAMED
    7 results · 20ms · 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 ×

    TOBRAMYCIN FLEX REAGENT CARTRIDGE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    FLEXITOUCH SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Nitrile Powder Free Examination Glove with Low Dermatitis Potential Claim and Tested for Use with Chemotherapy Drugs (Blue)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 14, 2013

    LANCET DEVICE MMT-395 QCKSRTR M4 13L

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code KZH·January 11, 2011

    CELLEX PROCEDURAL KIT

    FDA Adverse Event
    Malfunction ·THERAKOS, INC.·Product code LNR·July 17, 2014

    Medtronic INTREPID Spinal System SPACER M 37X27, 8 DEG, Size 10MM, Part Number: REF 7962810; 12MM, REF 7962812; 14MM, REF 7962814; 16MM, REF 7962816; 18MM, REF 7962818; 20MM, REF 7962820; USA, Rx only, STERILE R. The INTREPID Spinal System is indicated for use with autogenous bone graft in patients with degenerative disc disease.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code MAX·February 6, 2009