BEUDAMED
    7 results · 36ms · 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.
    Filters FDA Adverse Event ×

    I-STAT EG7+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code CHL·April 11, 2019

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 15, 2025

    I-STAT B-HCG CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code DHA·January 22, 2019

    COBE CENTRYSYSTEM 3

    FDA Adverse Event
    Malfunction ·GAMBRO HEALTHCARE·Product code FII·April 10, 1999

    AUTO SUTURE MULTIFIRE ENDO GIA 45-3.5 DISPOSABLE LOADING UNI

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GCJ·September 3, 1997

    2024841-2001-00001

    FDA Adverse Event
    Other ·Product code BTO·March 2, 2001

    I-STAT B-HCG CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code DHA·February 6, 2019