BEUDAMED
    7 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 ×

    ACUFEX SUTURE RETRIEVER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867138391·DARRACH ELEVTR,10"LX5/8"W,BLNT W SERR

    SURECATH PORT ACCESS CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DADE URINE CHEMISTRY CONTROL LEVELS I AND II

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SCREW LOCKING

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·January 23, 2013

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·November 10, 2010

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 10, 2014