BEUDAMED
    8 results · 20ms · 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 ×

    NuVasive® Modulus TLIF Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VIPI BLOCK

    FDA 510(k)
    FDA Class 2 ·Dental

    SNAP WOUND CARE SYSTEM

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

    GMK-HINGE FEMORAL COMPONENT SIZE 3 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·July 25, 2022

    FLEXIBLE SHAFT (TRI-SHANK)

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code KWA·June 5, 2013

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·January 7, 2011

    COBAS INTEGRA 400

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·September 19, 2008

    ANALYTICAL E MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·July 19, 2013