BEUDAMED
    8 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 ×

    RESCUE MASK & CPR VALVE FOR MOUTH-TO-MASK TYPE CPR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TAPE, ELASTOPLAST ELASTIC TEAR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GMC Upper Arm Automatic Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TI COLLAR FOR 6MM DUAL-OPENING IMPLANTS

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·June 18, 2014

    GEMSTAR BOLUSCORD (EACH)

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·October 12, 2010

    ARCHITECT IPTH

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code CEW·December 20, 2012

    dS Breast 7ch 3.0T

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·December 4, 2024

    OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial Components (Product Line: 02-012-38-XXXX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021