BEUDAMED
    9 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 ×

    DiaTemp

    FDA 510(k)
    FDA Class 2 ·Dental

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583033082·ET20, KIT 312 NFM PB R BE ENCHANT 20

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780419198·Integra® Miltex® House-Bellucci Ear Scissors 3-...

    SIGMA STERILIZATION POUCH & ROLL

    FDA 510(k)
    FDA Class 2 ·General Hospital

    REPROCESSED ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ONE TOUCH ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·March 25, 2010

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·January 13, 2014

    PLV-100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·June 20, 2013

    UNICEL® DXC SYNCHRON ® CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·August 4, 2011