BEUDAMED
    10,000 results · 34ms · 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 ×

    HFG 350, 650, 1050

    FDA 510(k)
    FDA Class 2 ·Radiology

    SUPERCUT MAYO SCS 6-3/4 STR

    FDA Adverse Event
    Malfunction ·J. JAMNER SURGICAL INSTRUMENTS·Product code HFG·January 28, 2010

    MONOPOLAR CABLE 10 FEET

    FDA Adverse Event
    Malfunction ·J. JAMNER SURGICAL INSTRUMENTS·Product code HFG·June 11, 2010

    ACESSA GUIDANCE HANDPIECE

    FDA Adverse Event
    Injury ·ACESSA HEALTH INC.·Product code HFG·December 19, 2017

    ACESSA GUIDANCE HAND PIECE

    FDA Adverse Event
    Injury ·ACESSA HEALTH INC.·Product code HFG·December 20, 2017

    ACESSA PROVU HANDPIECE

    FDA Adverse Event
    Injury ·ACESSA HEALTH INC.·Product code HFG·December 14, 2021

    GYNECARE X-TRACT MORECELLATOR

    FDA Adverse Event
    Malfunction ·MEDSOURCE TECHNOLOGIES·Product code HFG·March 29, 2002

    5600040-6500JQD REUSE J HOOK

    FDA Adverse Event
    Malfunction ·DAVOL, INC. (RI)·Product code HFG·February 21, 2002

    ACESSA PROVU HANDPIECE

    FDA Adverse Event
    Injury ·ACESSA HEALTH INC.·Product code HFG·December 28, 2021

    ACESSA PROVU HANDPIECE

    FDA Adverse Event
    Injury ·ACESSA HEALTH INC.·Product code HFG·December 14, 2021

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Injury ·MEDSOURCE TECHNOLOGIES·Product code HFG·October 16, 2003

    STORZ STEINER ELECTROMECHANICAL MORCILLATOR

    FDA Adverse Event
    Malfunction ·KARL STORZ ENDOSCOPY AMERICA, INC.·Product code HFG·October 17, 2003

    STANDARD NON-COATED LA[AROSCOPIC ELECTRODE L-HOOK

    FDA Adverse Event
    Injury ·CONMED CORPORATION·Product code HFG·July 16, 2015

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Injury ·MEDSOURCE TECHNOLOGIES·Product code HFG·September 11, 2003

    CABLE, MONOPOLAR OPTIMA

    FDA Adverse Event
    Malfunction ·ACMI CORPORATION·Product code HFG·July 1, 2003

    CABLE, MONOPOLAR OPTIMA

    FDA Adverse Event
    Malfunction ·ACMI CORPORATION·Product code HFG·July 1, 2003

    SOLID SHAFT ELEC. "L" HOOK, 32 CM.

    FDA Adverse Event
    Other ·CONMED CORP.·Product code HFG·July 17, 2000

    CONMED

    FDA Adverse Event
    Injury ·CONMED·Product code HFG·June 8, 2000

    GYNECARE LAPAROSCOPIC MORCELLATOR

    FDA Adverse Event
    Injury ·GYNECARE INNOVATION CENTER·Product code HFG·April 10, 2000

    GYNECARE

    FDA Adverse Event
    Injury ·GYNECARE·Product code HFG·April 10, 2000