BEUDAMED
    22 results · 23ms · 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 Status: Injury ×

    6000036-1999-00075

    FDA Adverse Event
    Injury ·Product code DTK·July 29, 1999

    EF1

    FDA Adverse Event
    Injury ·MEDSHAPE, INC.·Product code KTT·March 11, 2025

    GREENFIELD 12FR SS VENA CAVA FILTER

    FDA Adverse Event
    Injury ·MEDI-TECH A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code DTK·November 17, 1999

    STYLE 68 SALINE FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FWM·May 23, 2025

    SMART CONTROL NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIO·February 14, 2008

    ULTRA-THIN BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·MEDI-TECH A DIV OF BOSTON SCIENTIFIC CORP.·Product code LIT·August 13, 1998

    SYMPHONY BILIARY STENT

    FDA Adverse Event
    Injury ·MEDI-TECH A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code FGE·February 14, 2000

    SYMPHONY BILIARY STENT

    FDA Adverse Event
    Injury ·MEDI-TECH A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code FGE·February 14, 2000

    SYMMETRY SMALL VESSEL BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·MEDI-TECH A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code LIT·August 13, 1998

    SYMPHONY BILIARY STENT

    FDA Adverse Event
    Injury ·MEDI-TECH A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code FGE·October 22, 1999

    BLUE MAX BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·MEDI-TECH A DIV OF BOSTON SCIENTIFIC CORP.·Product code LIT·July 20, 1999

    BLUE MAX BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·MEDI-TECH A DIV OF BOSTON SCIENTIFIC CORP.·Product code LIT·July 20, 1999

    MARSHAL BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·MEDI-TECH A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code LIT·October 22, 1999

    ULTRA-THIN BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·MEDI-TECH/A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code LIT·May 31, 2000

    SINGLE USE ELECTROSURGICAL HEMOSTATIC FORCEPS

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·November 13, 2023

    SINGLE USE ELECTROSURGICAL KNIFE KD-612

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·November 13, 2023

    XXL BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·MEDI-TECH A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code LIT·December 9, 1999

    EVIS LUCERA SMALL INTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDA·November 13, 2023

    SINGLE USE ELECTROSURGICAL KNIFE

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·November 13, 2023

    ICAST COVERED STENT SYSTEM, 6MMX22MMX120CM

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code PRL·April 28, 2025