BEUDAMED
    26 results · 38ms · 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 ×

    TCAT TKA Instrument Tray Set

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777648·LUMBAMED BASIC DORSAL STAYS M SILVER II

    Ceramco® iC

    FDA UDI
    Dentsply International Inc.·D00142006320·CC-312

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694017800·MFx 2.4mm Angulated Locking Reconstruction Orga...

    Olympus

    FDA UDI
    Gyrus ACMI, LLC·00821925047273·ES-IP iOR BWK Hamburg OP (no rack)

    Apelo® / Apelo® MIS

    FDA UDI
    ATLAS SPINE, INC.·M68120063200000·Tab Removal Tool

    0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENGUARD REMOTE PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 18, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 18, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 18, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 18, 2008

    DEEP BRAIN STIMULATON LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 18, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 18, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 18, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 18, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 18, 2008

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·August 11, 2011

    DEPUY ASR XL FEM IMP SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.·Product code KXA·July 1, 2013