BEUDAMED
    9 results · 18ms · 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 ×

    SYNTHES ELASTIC INTRAMEDULLARY NAIL (EIN) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERSAPOD (TM) INSTRUMENT TRAYS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PTH RIA

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 6, 2013

    OBGYN STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM DE MEXICO S DE RL DE CV·Product code FPO·January 13, 2011

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 31, 2014

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·July 25, 2025

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·December 24, 2024

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·December 24, 2024