BEUDAMED
    12 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.
    Filters Regulation: Us FDA ×

    DEPUY ACE SPIDER PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    WaveLight FS200 Patient Interface

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

    510 CARBINETTE X-RAY UNIT

    FDA 510(k)
    FDA Class 2 ·Radiology

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEO·June 19, 2006

    COULTER® ACT DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC·Product code GKZ·December 7, 2010

    TORNIER AEQUALIS REVERSE SHOLDER PROSTHESIS

    FDA Adverse Event
    Malfunction ·TORNIER INC.·Product code HSD·June 18, 2009

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·March 5, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC SINGAPORE OPERATIONS·Product code NVZ·August 7, 2014