BEUDAMED
    7 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 ×

    LDH-L

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M3848134960·Zip® Implant, 11 mm diam.

    VIRTURE MALE SLING SYSTEM WITH ALEXIS WOUND RETRACTOR CONVENIENCE KIT

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

    MODIFICATION TO SKYLIGHT IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    RECAP CEMENT FMRL HD RESUR 48M

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KXA·May 15, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·October 31, 2012

    NOT APPLICABLE (INCIDENT OCCURRED IN WAREHOUSE)

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·August 24, 2010