BEUDAMED
    173 results · 23ms · Sources: EU EUDAMED, US FDA

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    Nitrile Powder Free Examination Gloves Tested for Use with Chemotherapy Drugs-Violet Blue (VBLU)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CAPIOX RX15 HOLLOW, FIBER OXYGENATOR WITH/WITHOUT HARDSHELL RESERVOIR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MICRO PLATE, L-SHAPE, 100, LEFT, LONG, CP TITANIUM

    FDA Adverse Event
    Malfunction ·KARL LEIBINGER MEDIZINTECHNIK·Product code HRS·July 3, 1997

    MICRO PLATE, Y-SHGAPE, LONG, CP TITANIUM

    FDA Adverse Event
    Malfunction ·KARL LEIBINGER MEDIZINTECHNIK·Product code HRS·July 3, 1997

    AUTO SUTURE PREMIUM PLUS CEEA 31

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL CORPORATION·Product code GAG·March 13, 1997

    RESTORE 3.3X10 SELF-TAP IMPLANT W/MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 10, 1998

    MENTOR 350-1640

    FDA Adverse Event
    Injury ·MENTOR H/S·Product code FWM·July 17, 1998

    RESTORE 3.3X15 SELF-TAP+

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·February 5, 1998

    AUTO SUTURE CHEMOSITE IMPLANTABLE VENOUS ACCESS

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL CORP.·Product code LJT·April 15, 1997

    RESTORE 6X8 SELF-TAPPING IMPLANT W/MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 4, 1998

    TARGET TIP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·March 10, 1997

    AUTO SUTURE CHEMOSITE IMPLANTABLE ARTERIAL ACCESS SYSTEM

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code LJT·June 19, 1997

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO.·Product code MGB·September 17, 1997

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·April 21, 1999

    AUTO SUTURE TA LONG 90-3.5

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORPORATION·Product code GAG·November 18, 1997

    AUTO SUTURE PREMIUM PLUS CEEA 31MM

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·November 18, 1997

    AUTO SUTURE ENDO CLIP II M/L

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GCJ·September 29, 1997

    CARPENTIER-EDWARDS PHYSIO ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP./EDWARDS CVS DIVISION·Product code KRH·September 3, 1997

    AUTO SUTURE PREMIUM MULTIFIRE TA 90-3.5

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·November 24, 1997