BEUDAMED
    31 results · 24ms · Sources: EU EUDAMED, US FDA

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    VarseoSmile Crown plus

    FDA 510(k)
    FDA Class 2 ·Dental

    DJO SURGICAL

    FDA UDI
    Encore Medical, L.P.·00190446819905·SPECIAL, EMPOWR ADJ. TIBIAL KINEMATIC ALIGNMENT...

    Dornier Thulio Performance Fiber

    FDA UDI
    INNOVAQUARTZ LLC·00816959021931·

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116023349·270 Micron SU Thulio Performance Ball-Tip 3m Fiber

    Classic by RISKONTROL

    FDA UDI
    ACTEON MANUFACTURING·03760243000539·Disposable single use tips for air/water syringe.

    6450 RV2 MASK

    FDA UDI
    HANS RUDOLPH, INC.·00874750004911·DISP V2 XS FACE PC/HG/MASK ADP

    NA

    FDA UDI
    Synthes GmbH·10886982142344·2.4MM CORTEX SCREW SELF-TAPPING 38MM

    GLOBAL SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NITRILE EXAMINATION GLOVES POWDERFREE (BLUE COLOR)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 12, 2024

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 5, 2016

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·December 6, 2011

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·December 14, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 27, 2014

    REPLY

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA S.R.L.·Product code NVZ·June 28, 2013

    ACCURUS 800CS

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·August 4, 2011

    HAMILTON-C6

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·February 10, 2025

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·February 20, 2017

    COREVALVE REVALVING SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·January 17, 2017