BEUDAMED
    8 results · 19ms · 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 ×

    Mano and Mano Personal Lubricant

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    AMC

    FDA UDI
    Advantage Medical Electronics, LLC·00849593062596·1 Tube NIBP Hose, Philips (Agilent/HP), 5'

    OPTICATH CENTRAL VENOUS OXIMETRY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    K-Y BRAND LONG LASTING VAGINAL MOISTURIZER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 8, 2024

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 14, 2011

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 11, 2013

    ENDOPATH XCEL DILATING TIP TROCAR WITH STABILITY SLEEVE - 12MM DIAMETER, 100MM

    FDA Adverse Event
    Death ·ETHICON ENDO-SURGERY, LLC·Product code GCJ·September 16, 2008