BEUDAMED
    8 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.

    BRAUN TRAVEL

    FDA 510(k)
    FDA Class 1 ·Dental

    NA

    FDA UDI
    Zimmer, Inc.·00889024273733·

    48CH Head Coil

    FDA 510(k)
    FDA Class 2 ·Radiology

    XPS 3000 SYSTEM WITH RECIPROCATING ADAPTER AND SUCTION CANNULAE

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

    ZIMMER M/L TAPER KINECTIV FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWA·March 30, 2016

    SITTER ELITE

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·March 24, 2014

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    SPIROS CONNECTOR

    FDA Adverse Event
    Other ·ICU MEDICAL, INC.·Product code FPA·July 27, 2010