BEUDAMED
    8 results · 21ms · 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 ×

    Dia-X Bond Universal

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526159594·PROTECT.GENU KNEE SUPPORT GRAY IV

    ELMED INCORPORATED

    FDA UDI
    ELMED INCORPORATED·00842180121164·8 MM DIA., 30 CM, ELMED LAPAROSCOPE, 450 VIEWIN...

    AUTO SUTURE PREMIUM PLUS CEEA DISPOSABLE STAPLER

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

    CIANNA MEDICAL TISSUE MARKER AND DELIVERY SYSTEM

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

    SWAN-GANZ CONTINUOUS CARDIAC OUTPUT CATHETER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code DYG·October 30, 2008

    UNISOLVE WIPES

    FDA Adverse Event
    Injury ·SMITH & NEPHEW WOUND MANAGEMENT·Product code KOX·August 23, 2011

    M2A 38MM MODULAR HEAD -3MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 11, 2013