BEUDAMED
    27 results · 24ms · 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 ×

    STERILE BUTTON PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Accu-Patch Gold Plated type with Clear Tape

    FDA UDI
    SAKAMURA KENKYUSHO, K.K.·04955114013094·300 units in single package

    Soft-Form™ Thermo Plastic External Nasal Splint

    FDA UDI
    INVOTEC INTERNATIONAL, INC.·00818501022625·Soft-Form™ Thermo Plastic External Nasal Splint...

    Sense System with IBT Electrodes

    FDA UDI
    INFINITE BIOMEDICAL TECHNOLOGIES, LLC·00850004850459·Surface electrodes for Electromyography with Pa...

    D-SPECT® Cardio

    FDA UDI
    SPECTRUM DYNAMICS MEDICAL, INC·07290108670073·Single Photon Emission Computed Tomography syst...

    Kalitec Special

    FDA UDI
    Kalitec Direct LLC·B073DRK0100210·SNII Awl Tap, 5.50mm

    Matira

    FDA UDI
    Kalitec Direct LLC·B07307K0100210·Assembly, Caddie, Plates and Screws, Hinged

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0100210·Caddie Lid, Rods, 5.5mm

    OXYGEN APPLIED SYMPTOM IMPROVEMENT SYSTEM (OASIS)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    IMMAGE IMMUNOCHEMISTRY SYSTEM LIPOPROTEIN(A) LPAX REAGENT, ARRAY SYSTEM LIPOPROTEIN(A) LPA REAGENT, LIPOPROTEIN(A) CALIB

    FDA 510(k)
    FDA Class 2 ·Immunology

    ADVIA CENTAUR XP TNI-ULTRA ASSAY

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·October 23, 2017

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·March 19, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·March 1, 2011

    ENDO CATCH GOLD 10MM SPECIMEN POUCH INTL

    FDA Adverse Event
    Malfunction ·SANTO DOMINGO - USS·Product code GCJ·March 10, 2008

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 20, 2014

    2520274-2013-02987

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·May 31, 2013

    2520274-2013-02983

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·May 31, 2013

    2520274-2013-02985

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·May 31, 2013

    2520274-2013-02986

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·May 31, 2013

    2520274-2013-02979

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·May 31, 2013