BEUDAMED
    10 results · 29ms · Sources: EU EUDAMED, US FDA

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    Echelon Endopath Staple Line Reinforcement

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

    2008T HD SYS. W/O CDX W/BIBAG BLUE STAR

    FDA Adverse Event
    Malfunction ·CONCORD MANUFACTURING·Product code KDI·May 20, 2024

    2008T HD SYS. W/O CDX W/BIBAG BLUE STAR

    FDA Adverse Event
    Malfunction ·CONCORD MANUFACTURING·Product code KDI·February 29, 2024

    2008T HD SYS. W/O CDX W/BIBAG BLUE STAR

    FDA Adverse Event
    Malfunction ·CONCORD MANUFACTURING·Product code KDI·February 29, 2024

    2008T HD SYS. W/O CDX W/BIBAG BLUE STAR

    FDA Adverse Event
    Malfunction ·CONCORD MANUFACTURING·Product code KDI·March 19, 2024

    E-STATIS 40 SYSTEM

    FDA 510(k)
    FDA Class 1 ·Dental

    PC CARE BLOOD GLUCOSE DATA MANAGEMENT SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·October 9, 2008

    6000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 14, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·July 29, 2011