BEUDAMED
    473 results · 25ms · 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 Regulation: Us FDA ×

    VC10 PUMP, 115V

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code HHK·January 2, 2025

    ENDOSAMPLER

    FDA Adverse Event
    Injury ·MEDICAL GYN PRODUCTS·Product code HHK·July 8, 1996

    VACURETTE, CURVED 10MM 10/PKG

    FDA Adverse Event
    Malfunction ·ACMI CORPORATION·Product code HHK·March 19, 2004

    EXPLORA CURETTE 3MM WITH

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HHK·November 10, 2017

    PIPELLE

    FDA Adverse Event
    Malfunction ·UNK·Product code HHK·June 1, 2022

    VACURETTE "F" TIP 8MM 10/PKG

    FDA Adverse Event
    Malfunction ·ACMI CORPORATION·Product code HHK·December 15, 2003

    PIPELLE DE CORNIER MARK II

    FDA Adverse Event
    Injury ·LABORATORIES PRODIMED, ZI·Product code HHK·August 13, 2015

    PIPELLE DE CORNIER MARK II

    FDA Adverse Event
    Injury ·PRODIMED·Product code HHK·September 11, 2015

    VACURETTE CANNULA, BERKELEY CURVED 9 MM

    FDA Adverse Event
    Malfunction ·ACMI CORPORATION·Product code HHK·July 9, 2004

    BERKELEY SAFE-TOUCH 10/PKG TISSUE TRAPS

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code HHK·April 24, 2026

    3MM PIPET CURETTE BOX=50

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HHK·October 10, 2018

    WECK

    FDA Adverse Event
    Injury ·PILLING WECK·Product code HHK·March 12, 2013

    VACURETTE CURRETTE 12MM

    FDA Adverse Event
    Malfunction ·GYRUS MEDICAL, INC.·Product code HHK·December 19, 2008

    BERKELEY

    FDA Adverse Event
    Injury ·CABOT MEDICAL·Product code HHK·July 29, 1997

    SELECTCELLS STANDARD ENDOMETRIAL SAMPLING DEVICE

    FDA Adverse Event
    SELECT MEDICAL SYSTEMS, INC.·Product code HHK·October 9, 1996

    EXPLORA CURETTE 3MM WITH

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL INC.·Product code HHK·June 15, 2022

    VC10 PUMP, 115V

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code HHK·September 30, 2025

    UTERINE EXPLORA CURETTE - MODEL I

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code HHK·July 11, 2025

    VACURETTE CURETTE

    FDA Adverse Event
    Malfunction ·ACMI CORPORATION·Product code HHK·February 8, 2006

    VACURETTE

    FDA Adverse Event
    Malfunction ·ACMI CORPORATION·Product code HHK·January 24, 2006