BEUDAMED
    14 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 ×

    ODYSSEY HO:YAG SURGICAL LASER SYSTEMS & ACCESSORIES

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

    KOMET Surgical Saw Blade

    FDA UDI
    Gebr. Brasseler GmbH & Co. KG·14053613274729·

    KOMET Surgical Saw Blade

    FDA UDI
    Gebr. Brasseler GmbH & Co. KG·14053613274620·

    KOMET Surgical Saw Blade

    FDA UDI
    Gebr. Brasseler GmbH & Co. KG·14053613064306·

    KOMET Surgical Saw Blade

    FDA UDI
    Gebr. Brasseler GmbH & Co. KG·14053613049853·

    MAXISONIC FAMILY AND SWIFT ULTRASONIC SCALER

    FDA 510(k)
    FDA Class 2 ·Dental

    Ultrasound Scanner System BK2300

    FDA 510(k)
    FDA Class 2 ·Radiology

    ENRHYTHM

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·February 9, 2013

    GEMINI STONE RETRIEVAL PAIRED WIRE / HELICAL BASKET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FFL·January 7, 2011

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE INC.·Product code LZG·July 7, 2014

    VANGUARD (TM) CR FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·November 1, 2019

    VANGUARD (TM) DCM TIBIAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·November 1, 2019

    BIOMET SERIES A STANDARD PATELLA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRY·November 1, 2019

    BIOMET TIBIAL PLATE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRY·November 1, 2019