BEUDAMED
    13 results · 22ms · 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 ×

    THEKEN VU MESH VBR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Rotex / Rotex-RD / Dalbo®-Rotex

    FDA UDI
    Cendres+Métaux SA·07640166514725·Rotex / Rotex-RD / Dalbo®-Rotex Root canal dril...

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·November 19, 2007

    D.SIGN 30

    FDA 510(k)
    FDA Class 2 ·Dental

    EXPANDABLE KNEE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·December 3, 2007

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 25, 2025

    LINEAR 3-6

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 13, 2024

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE SJ·Product code JPA·December 10, 2007

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·April 22, 2013

    INFRAVISION URETERAL KIT

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code EZN·April 18, 2011

    NOVA MAX GLUCOSE MONITOR

    FDA Adverse Event
    Malfunction ·NOVA BIOMEDICAL CORP.·Product code NBW·July 3, 2008

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012