BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    IMMULITE PROGESTERONE

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CONCISE LIGHT CURED WHITE SEALANT

    FDA 510(k)
    FDA Class 2 ·Dental

    BIOSELF 2000 FERTILITY INDICATOR

    FDA 510(k)
    FDA Unclassified ·Unknown

    AED PRO

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 9, 2013

    PLMA DVC V11.51 1 N

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·December 6, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 18, 2014

    JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023

    JAWS "HIQ+", 5 X 330 MM, SCISSORS, METZENBAUM

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 30, 2023

    SHAFT "HIQ+", 5 X 330 MM

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·May 23, 2023

    JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023