BEUDAMED
    9 results · 33ms · 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.

    MICROTRAK CHLAMYDIA EIA

    FDA 510(k)
    FDA Class 1 ·Microbiology

    OPTICS ONE

    FDA UDI
    MEDICAL TECHNIQUE, INC.·00815384022025·Laser/Video Camera Drape 6 x 96 Elastic End

    MONOJECT ARTERIAL BLOOD SAMPLING DEVICE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    EG-3670URK

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    M2A-MAGNUM MOD HEAD SZ 52MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 24, 2014

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·October 22, 2010

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·December 28, 2012

    Angiotech Pediatric Bone Marrow Needle. Pediatric Bone Marrow Needle. STERILE. Product Number: ION18015. 510k K980196. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended Use: Pediatric Bone Marrow Needle

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code KNW·September 1, 2009

    Bivona Aire-Cuf Endotracheal Tube

    FDA Enforcement
    Class II ·Terminated·Smiths Medical ASD Inc.·November 3, 2021