BEUDAMED
    8 results · 23ms · 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 ×

    KIRWAN SURGICAL PRODUCTS, INC. MODEL 28 1500 ELECTROSURGERY GENERATOR

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

    Modulus

    FDA UDI
    Nuvasive, Inc.·00195377049865·Modulus ALIF HL Trial, 12x38x30mm 25°

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091982176·posteriors; shade A3.5 light; size XL; upper jaw

    LTM-BPS SURGICAL MESH

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

    Polychloroprene Powder Free Sterile Surgical Gloves, White, Tested for Use with Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    SARA 3000

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH POLSKA SP. ZO.O.·Product code FSA·February 22, 2013

    J-VAC RESERVOIR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code KOG·January 18, 2011

    ZEPHYR XL SR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·September 27, 2016