BEUDAMED
    7 results · 17ms · 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.

    CARBON DIOXIDE REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PELVIS BELLYBOARD PLUS PATIENT POSITIONING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    TERASON USMART3300 ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    9MM/125 DEG TI CANN TFNA 340MM/LEFT - STERILE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HSB·April 27, 2018

    ARIS TRANS-OBTURATOR

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FTL·January 30, 2014

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 20, 2012

    RESTOR ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 17, 2010