BEUDAMED
    557 results · 27ms · Sources: EU EUDAMED, US FDA

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    VitriGuard

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526743748·ACHIMED ACHILLES SUPP SAND V

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526785045·EPICOMED ELB SUPPORT SAND V

    GORNEY SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896055810·GORNEY SCISSORS CURVED DOUBLE BEVELED BLADES PO...

    NA

    FDA UDI
    aap Implantate AG·04042409049279·K-wire with 2 trocar points, ø0.8, L 150

    BACT/ALERT FN CULTURE BOTTLE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AUTOPULSE® LIFEBAND

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·October 24, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 2, 2013

    ULTRAFLEX TRACHEOBRONCHIAL STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC IRELAND, LTD.·Product code JCT·May 21, 2008

    ULTRAFLEX TRACHEOBRONCHIAL STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC IRELAND, LTD.·Product code JCT·May 21, 2008

    ENDOSTAT II ELECTROSURGICAL UNI

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·September 3, 2008

    ICY HOT

    FDA Adverse Event
    Injury ·CHATTEM, INC.·Product code IMD·March 4, 2008

    BD VACUTAINER ECLIPSE BLOOD COLLECTION NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·December 5, 2019

    HIRES 90K

    FDA Adverse Event
    Injury ·ADVANCED BIONICS LLC·Product code MCM·December 23, 2008

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

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

    RF 3000 GENERATOR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEI·May 23, 2008

    ULTRAFLEX COVERED NG ESOPHAGEAL STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC IRELAND, LTD·Product code ESW·April 9, 2008

    ULTRAFLEX TRACHEOBRONCHIAL STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC IRELAND, LTD.·Product code JCT·April 7, 2008