BEUDAMED
    232 results · 32ms · 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 ×

    SIRION Lateral Lumbar Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Bernafon

    FDA UDI
    Bernafon AG·05711584086803·ZR3, KIT 312 NFM 75 R BE ZERENA 3

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694009560·2.0mm x 6mm Cannulated Lag Screw

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776199821·LLETZ GRAVES SPEC LG wEvac

    CETRA

    FDA UDI
    Orthofix US LLC·18257200137428·CETRA - 2.0 SCREW CADDY, CONSTRAINED SCREWS

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694070041·Cannulated 2.0 x 6mm Lag Screw Sterile Qty 5

    HAMILTON-TC1

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CRYOMEGA

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

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·August 21, 2006

    ACDF STAND ALONE CERVICAL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·October 8, 2025

    COBAS INTEGRA 400+

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 6, 2007

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·May 24, 2006

    SABINA

    FDA Adverse Event
    Other ·LIKO, INC.·Product code FSA·November 16, 2006

    KENDALL DOVER

    FDA Adverse Event
    Other ·TYCO HEALTHCARE/KENDALL·Product code EZL·June 27, 2006

    N-550 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT, INC.·Product code DQA·May 24, 2006

    PHILOS II DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code DXY·May 24, 2006

    KENDALL DOVER

    FDA Adverse Event
    Other ·TYCO HEALTHCARE/KENDALL·Product code EZL·June 27, 2006

    ACDF STAND ALONE CERVICAL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·April 25, 2025

    3CC SAF. SYR 20X1-1/2

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE/KENDALL·Product code MEG·January 4, 2007

    SPINAL ANESTHESIA TRAY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code CAZ·December 21, 2006