BEUDAMED
    10 results · 18ms · 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 ×

    TriMed Wrist Fixation System 3

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Packout-5 - Class A First Aid Kit - Poly

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588226378·Packout-5 - Class A First Aid Kit - Poly

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·10887488055565·BIOPSY PROCEDURE PACK

    SUMMIT MEDICAL, INC.

    FDA registration
    SUMMIT MEDICAL, INC.·1 product·🇺🇸 United States

    LITE DECOMPRESSION SYSTEM- LIGHT CABLE MODEL 48089999

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

    BD-3000 MICROKERATOME SYSTEM, MODEL K-3000 MICROKERATOME

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code ITI·November 4, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 25, 2011

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 12, 2013

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Right, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-32, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-33, c) 44, 47, 50, 53 head, Large, Item Number 314-13-34, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-35; Shoulder Arthroplasty

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