BEUDAMED
    24 results · 23ms · 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 ×

    Plastic LOR Syringe

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·04049958003127·400 micron Holmium Laser Fiber Cable, Single Us...

    AGXO

    FDA UDI
    Oticon A/S·05707131356635·G400 S, MINIRITE R LI-ION 2.4G C092 AGXO

    LIPOSUCTION CANNULA

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B0992013560·LIPOSUCTION CANNULA SPATULATED TIP

    Liposuction Cannula

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896108141·Liposuction Cannula Spatulated 220 X 3 Millimet...

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383534468·"An absorbent paper points is an endodontic pap...

    ONTRAK TESTCUP PRO-5, MODEL 1986678

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    THE DIVACUP MENSTRUAL SOLUTION

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    HAMILTON-C3

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·February 9, 2024

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

    GREENLIGHT HPS BPH FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·June 26, 2013

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·August 11, 2011

    CONTOUR TRANSTAR STAPLER SET

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 6, 2018

    CONTOUR TRANSTAR STAPLER SET

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 2, 2018

    PROXIMATE*75MM LINEAR CUTTER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 2, 2018

    UNKNOWN_PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·December 19, 2013

    JETSTREAM® ATHERECTOMY CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MCW·February 17, 2016

    CONTOUR TRANSTAR STAPLER SET

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 27, 2018

    INTERVERTEBRAL FUSION DEVICE W/INTEGRATED FIXATION,CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code OVE·January 27, 2017