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 ×

    ANGIODYNAMICS, INC., PERCUTANEOUS INTRODUCER AND ELVS PROCEDURE KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HARMONE-SCHWARZER EEG SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE

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

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 8, 2013

    AS50 INFUSION PUMP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·December 13, 2007

    FIRM

    FDA Adverse Event
    Injury ·HISTORICAL CPI ST. PAUL·Product code NVN·April 6, 2011

    BD FACS¿ 7-COLOR SETUP BEADS 25 TESTS

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code OYE·May 8, 2025

    TRULIANT TIB IMP PS INSERT SZ 3 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 5, 2022

    BD FACS¿ 7-COLOR SETUP BEADS 25 TESTS

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code OYE·March 28, 2025

    Smith & Nephew FOOTPRINT Ultra PK Suture Anchor, 5.5mm Part Number: 72202902

    FDA Enforcement
    Class II ·Ongoing·Smith & Nephew, Inc.·April 29, 2020