BEUDAMED
    9 results · 30ms · 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 ×

    PHOENIX HEMODIALYSIS DELIVERY SYSTEM, VERSION 3.35

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Paltop

    FDA UDI
    PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108699678·Implant Insertion Key NP + Conical, Wide, Short

    EZ-SCOPE AN & EZ-SCOPE AN LITE

    FDA 510(k)
    FDA Class 1 ·Radiology

    INPLANT ORTHODONTIC ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    ACCURUS 800CS

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·April 17, 2013

    ARCHITECT TOTAL B-HCG

    FDA Adverse Event
    Malfunction ·A.I.D.D LONGFORD·Product code DHA·April 27, 2011

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 1, 2008

    EDWARDS LOCKING SYRINGE

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code MAV·June 16, 2023

    EDWARDS LOCKING SYRINGE

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES LLC·Product code MAV·March 29, 2022