BEUDAMED
    26 results · 22ms · Sources: EU EUDAMED, US FDA

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    LEGION POROUS + HA TIBIAL BASEPLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BLALOCK AORTA CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896010543·BLALOCK AORTA CLAMP SMOOTH FLEXIBLE JAW

    BLALOCK FLEXIBLE CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921008970·BLALOCK FLEXIBLE CLAMP SMOOTH JAW

    Spooled Nitanium

    FDA UDI
    Ortho Organizers, Inc.·00190707101046·.018 SPOOLED NITANIUM 10ft

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019315060441·

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019315060458·

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019315107214·

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019315060434·

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019315107207·

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019315107191·

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA INTL.·Product code MNI·October 14, 2011

    CALIBRITE PERCP-CY5.5 BEADS AND FACSCOMP SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Hematology

    MERIDIAN-PORTABLE

    FDA 510(k)
    FDA Class 2 ·Neurology

    Widex

    FDA UDI
    Widex A/S·05706069773644·Widex EVOKE E-FA, Telecoil, Volume control, RC ...

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA INTERNATIONAL·Product code MNI·November 11, 2011

    UniPerc(R) Adjustable Flange Tracheostomy Tube kit, Reorder Number 100/897/080 CZ The UniPerc(R) Tracheostomy Tubes can be used during the surgical placement of a stoma or as a replacement tube to an already existing stoma for patients with larger necks. The tracheostomy tubes are removed and may be replaced after no more than 30 days with an identical device. The range may include the following configurations: cuffed or uncuffed tracheostomy tubes, tracheostomy tube inner cannula, cleaning brushes and tracheostomy tube holder.

    FDA Recall
    Terminated ·Smiths Medical ASD Inc.·Product code JOH·August 14, 2017

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013

    CARE ASSIST BED

    FDA Adverse Event
    Malfunction ·HILL-ROM PLUVIGNER·Product code FNL·July 31, 2014

    KIMVENT CLOSED SUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·KIMBERLY-CLARK HEALTH CARE·Product code BSY·May 24, 2011

    HAHN TAPERED IMPLANT Ø5.0 X 10 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT INC.·Product code DZE·November 14, 2024