BEUDAMED
    11 results · 24ms · 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 Regulation: Us FDA ×

    HEMOSIL RECOMBIPLASTIN 2G (8 ML VIAL)

    FDA 510(k)
    FDA Class 2 ·Hematology

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019517075595·

    NORIAN DRILLABLE INJECT, NORIAN DRILLABLE FAST SET PUTTY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRIGEN STRAIGHT HUMERAL NAIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

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

    CONCORDE PROTI 5 DG, 9X8X27 MM

    FDA Adverse Event
    Injury ·TYBER MEDICAL·Product code MAX·July 18, 2023

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code MMI·May 29, 2013

    JUVEDERM (VOLUME/CONCENTRATION UNKNOWN)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·September 29, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 17, 2011

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·August 21, 2023

    Eversense CGM SENSOR (FG-4200-00-301)-Continuous Glucose Monitor

    FDA Enforcement
    Class II ·Terminated·Senseonics, Inc.·November 6, 2019