BEUDAMED
    10 results · 21ms · 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 ×

    LOQTEQ DISTAL LATERAL FEMUR PLATE 4.5 (LEFT AND RIGHT VERSION) LOQREQ CORTICAL SCREW 4.5 T25, SELF-TAPPING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AF541

    FDA UDI
    Respironics, Inc.·00606959024502·AF541 Mask with Entrainment Elbow, Leak 1, with...

    MONOSYN VIOLET 2/0 (3) 70CM HRC26 (M)RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·March 14, 2022

    GDC POWER SUPPLY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - FREMONT·Product code HCG·July 20, 2010

    GDC POWER SUPPLY, MODEL GDC POWER SUPPLY: 451007-4

    FDA 510(k)
    FDA Class 2 ·Neurology

    HANDHELD PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWP·November 7, 2019

    OPTISENSE

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·January 13, 2014

    CORAIL2 LAT COXA VARA SIZE 11

    FDA Adverse Event
    Injury ·DEPUY FRANCE·Product code KWA·May 21, 2013

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·June 7, 2011