BEUDAMED
    9 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 ×

    STERNGOLD BIO-5 (1127210)

    FDA 510(k)
    FDA Class 2 ·Dental

    SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295242093·SIGMA TIBIAL INSERT ROTATING PLATFORM TC3 SIZE ...

    AUTOSUTURE MODIFIED VERSAPORT TROCAR WITH FIXATION SLEEVE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Pantheris Catheter, Lightbix HS Imaging Console, Lightbox Sled

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BONE ANCHOR SYSTEM FOR SOFT TISSUE SUPPORT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code MBI·April 27, 2012

    REF H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·August 9, 2016

    PRIMEADVANCED

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code LGW·February 14, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·January 7, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014