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 ×

    INSTRUCTION CHANGE FOR RIGHT ATRIAL/RAAF CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODEL 9500 ARGON, KRYPTON & DYE SURGICAL LASER SYS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SYVA SAMPLE SEAL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SELECTSECURE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVN·June 10, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 12, 2010

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·December 10, 2012

    SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024