BEUDAMED
    8 results · 18ms · 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.

    MB/BACT BLOOD CULTURE BOTTLE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    COLUMBUS REVISION KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    H.A.C. MODEL-A (ALL IN THE EAR)

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    AXIOM ARISTOS VX PLUS

    FDA Adverse Event
    Injury ·SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD·Product code MQB·April 7, 2021

    AS COLUMBUS REV F FEMUR ZEMENTIERT F5L

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·November 6, 2019

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 25, 2014

    SEE H-10

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·February 28, 2013

    RESERVOIR 1.8 ML MMT-326A

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code FRN·January 20, 2011