BEUDAMED
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    AMERICAN CATHETER CORP

    FDA registration
    AMERICAN CATHETER CORP·1 product·🇺🇸 United States

    american catheter CORP

    FDA UDI
    American Catheter Corp.·B80291000·laparoscopic cholangiogram catheter

    AMERICAN CATHETER

    FDA Adverse Event
    Malfunction ·AMERICAN CATHETER CORP·Product code GBZ·April 21, 2015

    AMERICAN CATHETER CORP

    FDA Adverse Event
    Injury ·AMERICAN CATHETER CORP·Product code LDD·August 13, 2004

    CHOLANGIOGRAPHY SET

    FDA Adverse Event
    Malfunction ·AMERICAN CATHETER CORP.·Product code DQO·February 11, 1994

    CATHETER, 4.0 FR

    FDA Adverse Event
    AMERICAN CATHETER CORP.·Product code FFL·December 23, 1993

    DISPOSABLE CYTOLOGY BRUSH

    FDA Adverse Event
    Malfunction ·AMERICAN CATHETER, CORP.·Product code BTG·August 14, 1995

    DISPOSABLE BRONCHOSCOPY FORCEPS

    FDA Adverse Event
    AMERICAN CATHETER CORP.·Product code HTD·January 24, 1996

    American Catheter / Cholangiogram Catheter 9100 Series.

    FDA Recall
    Terminated ·American Catheter Corp·Product code GBZ·March 17, 2015

    American Catheter / Cholangiogram Catheter 9100 Series.

    FDA Enforcement
    Class II ·Terminated·American Catheter Corp·July 29, 2015

    MedNet EC-REP GmbH

    Authorized representative
    🇩🇪 Germany·464 Manufacturers·5263 Devices

    Emergo Europe B.V.

    Authorized representative
    🇳🇱 Netherlands·900 Manufacturers·22100 Devices