BEUDAMED
    22 results · 23ms · Sources: EU EUDAMED, US FDA

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    AVALON ELITE MULTI-PORT VENOUS FEMORAL CATHETER, 20FR, 22FR, 24FR, 26FR, 28FR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WAKO AUTOKIT LP(A) & LP(A) CALIBRATOR/COBAS BIO

    FDA 510(k)
    FDA Class 2 ·Immunology

    GLYCOSAL II HBA 1C TEST

    FDA 510(k)
    FDA Class 2 ·Hematology

    BILOX PROSTHESIS HEAD 12/14 28MM L

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·May 23, 2014

    EXCIA L PLASMAPORE UCAP 8/10 SIZE 11MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    ISODUR PROSTHESIS HEAD 12/14 32MM L

    FDA Adverse Event
    Malfunction ·AESCULAP AG&CO KG·Product code LPH·August 7, 2014

    QUINTEX SEMICONSTRAINED SCREW 4.0X16MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012

    EXCIA PLASMAPORE-UCAP 8/10 SIZE 11MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code MEH·June 21, 2013

    EXCIA CEMENTED 8/10 SIZE 12MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code JDI·November 5, 2012

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 8, 2024

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 14, 2014

    BIOLOX PROSTHESIS HEAD 12/14 28MM M

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012

    BIOLOX PROSTHESIS HEAD 12/14 32MM L

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    BIOLOX PROSTHESIS HEAD 8/10 32MM M

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LZO·June 21, 2013

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    PATIENT SPECIFIC SPLINT ORTHOGNATHIC, INTERMEDIATE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWT·April 29, 2013

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 5, 2011

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR GALWAY·Product code NIM·July 23, 2008

    ISODUR PROSTHESIS HEAD 12/14 28MM M

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LPH·January 16, 2015