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

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    LINA LOOP

    FDA Adverse Event
    Other ·LINA MEDICAL APS·Product code KNF·April 27, 2010

    KRATZ ANGLED CAPSULE SCRAPER

    FDA Adverse Event
    Other ·CARDINAL HEALTH - DISTRIBUTION·Product code HNF·August 25, 2003

    BOVIE "HF CABLE"

    FDA Adverse Event
    Other ·RICHARD WOLF·Product code KNF·September 12, 2000

    IRIS SCS CVD S/S 4-1/2

    FDA Adverse Event
    Other ·CARDINAL HEALTH (SNOWDEN PENCER)·Product code HNF·September 14, 2004

    IRIS

    FDA Adverse Event
    Other ·MILTEX INSTRUMENT CO., INC.·Product code HNF·April 6, 1999

    LINA GOLD LOOP

    FDA Adverse Event
    Other ·LINA MEDICAL POLSKA·Product code KNF·June 7, 2013

    MONOPOLAR CABLE

    FDA Adverse Event
    Other ·BOWA-ELECTRONIC GMBH·Product code KNF·October 6, 2000

    LINA GOLD LOOP

    FDA Adverse Event
    Other ·LINA MEDICAL·Product code KNF·June 7, 2013

    LINA GOLD LOOP

    FDA Adverse Event
    Other ·LINA MEDICAL POLSKA·Product code KNF·June 7, 2013

    MILTEX

    FDA Adverse Event
    Other ·MILTEX INSTRUMENT CO., INC.·Product code HNF·July 25, 1997

    WOLF

    FDA Adverse Event
    Other ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code KNF·April 25, 1997

    ETHICON ENDO-SURGERY, INC.

    FDA Adverse Event
    Other ·ETHICON ENDO-SURGERY, INC.·Product code KNF·February 11, 2000

    9614969-1999-00003

    FDA Adverse Event
    Other ·Product code KNF·February 16, 2000

    CAMERON-MILLER

    FDA Adverse Event
    Other ·CAMERON-MILLER·Product code KNF·January 18, 2000

    IRIS, SUPER CUT, STRAIGHT, 4 1/2"

    FDA Adverse Event
    Other ·MILTEX INSTRUMENT CO. INC.·Product code HNF·February 12, 2001

    ENDOSHEARS

    FDA Adverse Event
    Other ·UNITED STATED SURGICAL CORP.·Product code KNF·July 14, 1994

    *

    FDA Adverse Event
    Other ·Product code KNF·November 26, 1999

    IRIS SCISSORS

    FDA Adverse Event
    Other ·AESCULAP CORP.·Product code HNF·June 10, 1994

    UROGYN

    FDA Adverse Event
    Other ·OMNITECH SYSTEMS, INC.·Product code KNF·September 30, 2013

    1415191-2001-00002

    FDA Adverse Event
    Other ·Product code KNF·May 23, 2001