BEUDAMED
    7 results · 25ms · 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.

    TRYPTIC SOY BROTH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ERA® Standard 11° Female

    FDA UDI
    STERNGOLD DENTAL LLC·00841549102196·ERA® Standard 11° Female. ERA abutments provid...

    Pioneer Elite Diode Laser

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

    Klassic Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 15, 2014

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    TOPAZ 22X20 EXPORT UK

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·June 2, 2015