BEUDAMED
    10 results · 19ms · 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 ×

    ERBE APC APPLICATORS, MODELS 20132-106, 20132-107, 20132-109, 20132-110, 20132-11, 20132-112,20132-113, 20132-114, 2013-

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Impella CP Introducer

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ION¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·March 7, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 4, 2011

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·August 8, 2014

    CLICKX-3D-HEAD F/PEDICSCR POST-OPEN TAN

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NKB·February 12, 2013

    CLICKX PEDICSCR Ø6.2 L50 TAN DBLUE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NKB·February 12, 2013

    CLICKX-3D-HEAD F/PEDICSCR POST-OPEN TAN

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NKB·February 12, 2013

    CLICKX-3D-HEAD F/PEDICSCR POST-OPEN TAN

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NKB·February 12, 2013