BEUDAMED
    24 results · 22ms · 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.

    MULTIPERFECTEMP CAUTERY

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Hader Bar® Processing Jig

    FDA UDI
    STERNGOLD DENTAL LLC·00841549118340·The Hader Bar Processing Jig is an anodized alu...

    neoWave C

    FDA UDI
    XENIX MEDICAL LLC·00818345023833·Cervical Inserter

    FETAL MONITOR MODEL FHM-1

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

    LIGASURE LAPAROSCOPIC SEALER DIVIDER MODEL LS1100

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BD 50ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·February 15, 2019

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 20, 2020

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 23, 2020

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 23, 2020

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 24, 2020

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 23, 2020

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 24, 2020

    8100 PUMP MODULE 9.17.0.22

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 5, 2020

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·April 25, 2014

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·November 12, 2007

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code MTA·October 23, 2012

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 29, 2020

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 4, 2020

    BD 50ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·March 6, 2019

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 29, 2020