BEUDAMED
    8 results · 17ms · 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.

    SUNBRONZE SB24C/65 ULTRA

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

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756732116·TUR BASIN PACK

    PHYNE-TOUCH (PATIENT EXAMINATION GLOVES)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CAM-WRAP(TM) NEW STERILIZATION PROCEDURE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL MANUFACTURING CORPORATION·Product code MVK·May 16, 2014

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code DZL·January 4, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·November 11, 2010

    Exactech Equinoxe REVERSE SHOULDER,36mm Humeral Liner: a) +0mm, Item Number 320-36-00, b) +2.5mm, Item Number 320-36-03; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024