BEUDAMED
    14 results · 23ms · 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.

    MAGLUMI 2000 25-OH Vitamin D

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    JOURNEY CR KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY)

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

    COMPRESSION/DISTRACTOR ROD F/LOCK HOLE Ø2.7

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWN·June 26, 2013

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (LARGE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·July 20, 2011

    KNIGHTSTAR 330

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·September 26, 2008

    COOK COPE-LOOP CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LJE·August 23, 2021

    ULTRATHANE SUPRAPUBIC CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KOB·August 23, 2022

    COOK COPE-LOOP CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LJE·March 17, 2022

    COOK COPE-LOOP CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LJE·March 17, 2022

    COOK COPE-LOOP CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LJE·March 17, 2022

    COOK COPE-LOOP CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LJE·March 17, 2022

    COOK COPE-LOOP CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LJE·August 23, 2021

    COOK COPE-LOOP CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LJE·July 21, 2021