BEUDAMED
    8 results · 29ms · 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 ×

    APOLIPOPROTEIN B IMMUNOTURBIDIEMETRIC KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    AFFINITY QS Q-SWITCHED ND:YAG LASER SYSTEM

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

    Radio Therapy Treatment Chair

    FDA 510(k)
    FDA Class 2 ·Radiology

    UNKNOWN DEPUY TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·February 8, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·December 14, 2010

    MONOCRYL (POLIGLECAPRONE 25) SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAN·July 22, 2014

    LARGE EX-FIX 11MM CRBN FBR ROD 250MM / MR-CONDITIONAL

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018

    LARGE EX-FIX 11MM CRBN FBR ROD 300MM / MR-CONDITIONAL

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018