BEUDAMED
    9 results · 21ms · 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.

    MSI 2002 SERIES BED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Snowden-Pencer

    FDA UDI
    CAREFUSION 2200, INC·10885403151347·AUFRICHT RETRACTOR CONCAVE BLADE OVERALL LENGTH...

    KAPPA SERUM (FREE) ANTI-HUMAN

    FDA 510(k)
    FDA Class 2 ·Immunology

    KIMBERLY-CLARK STERLING NITRILE POWDER-FREE EXAM GLOVE (STERILE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024199965·

    TERUMO CDI 540 CALIBRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·October 8, 2010

    LAMITRODE TRIPOLE 16

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 14, 2012

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code NVY·January 13, 2014

    dS Breast 7ch 3.0T

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·December 4, 2024