BEUDAMED
    8 results · 28ms · 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 ×

    Spine Wave Navigated Instruments

    FDA 510(k)
    FDA Class 2 ·Neurology

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780422747·Integra® Miltex® House Sickle Knife 6", 0.75mm ...

    BLO2X OXYGEN BLOCKER

    FDA 510(k)
    FDA Class 2 ·Dental

    TWINFIX ULTRA TI, TWINFIX ULTRA PK, TWINFIX ULTRA HA SUTURE ANCHORS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    I-STAT E3+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·March 31, 2020

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·June 3, 2013

    SOL SYS 8/12.0 LRG ST

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·October 22, 2014

    I-STAT 1 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE INC.·Product code JJE·June 30, 2011