BEUDAMED
    9 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 ×

    LOCKING SCREW, FULLY THREADED 5X45 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 30, 2009

    Praxiject™ 0.9% NaCl

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD BBL™ Sensi-Disc™ Ceftazidime/Clavulanic Acid 30/10 µg

    FDA UDI
    BECTON, DICKINSON AND COMPANY·30382902317549·BD BBL™ Sensi-Disc™ Ceftazidime/Clavulanic Acid...

    WONDFO COCAINE URINE TEST (COC 100), WONDFO CANNABINOIDS URINE TEST (THC 40)

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    FLEXISKIN POWDER FREE LATEX EXAMINATION GLOVES, NON STERILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 14, 2014

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·September 1, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·July 17, 2013

    Revogene, Catalog no. 610210. IVD test instrument

    FDA Enforcement
    Class II ·Ongoing·Meridian Bioscience Inc·August 3, 2022