BEUDAMED
    10 results · 20ms · 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 ×

    SYNCHRON SYSTEMS OP 300 LOW AND HIGH URINE CALIBRATORS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993022·anteriors; shade A1; mould UBXL

    Bipolar scissors

    FDA UDI
    SOPRO-COMEG GmbH·04059082014739·

    Retractable Safety Insulin Syringe

    FDA 510(k)
    FDA Class 2 ·General Hospital

    THE PICC WAND PEELABLE SAFETY INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024

    METRX SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·June 10, 2024

    DIMENSION VISTA® CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code MMI·March 7, 2013

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·February 7, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014