BEUDAMED
    20 results · 32ms · Sources: EU EUDAMED, US FDA

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    AccuMed Corp.

    FDA registration
    AccuMed Corp.·19 products·🇩🇴 Dominican Republic

    AccuMED Corp.

    FDA registration
    AccuMED Corp.·1 product·🇩🇴 Dominican Republic

    ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP.

    FDA registration
    ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP.·105 products·🇺🇸 United States

    SWAN NECK COIL-CATH

    FDA Adverse Event
    Malfunction ·ACCURATE SURGICAL INSTRUMENTS CORP.·Product code FJS·January 9, 1998

    SWAN NECK COIL-CATH

    FDA Adverse Event
    Injury ·ACCURATE SURGICAL INSTRUMENT CORP.·Product code FJS·January 9, 1998

    METZENBAUM SCISSORS

    FDA Adverse Event
    Malfunction ·ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP.·Product code LRW·October 13, 2017

    JEWELERS BIPOLAR FORCEP

    FDA Adverse Event
    Malfunction ·ACCURATE SURGICAL AND SCIENTIFIC INSTRUMENTS CORP.·Product code GEI·July 14, 1998

    MICROSUTURE SCISSORS

    FDA Adverse Event
    Malfunction ·ACCURATE SURGICAL AND SCIENTIFIC INSTRUMENT CORP.·Product code LRW·November 16, 1995

    FIBER OPTIC LIGHT CABLE 3.5MM X 2300MM; 7.5 FT.

    FDA Adverse Event
    Malfunction ·ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP.·Product code FCW·March 8, 2024

    SEMKIN BIPOLAR FORCEPS W/STOPS STR. 14CM, TIP 0.7MM DIA.

    FDA Adverse Event
    Malfunction ·ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP.·Product code GEI·May 29, 2025

    ASSI BLADE

    FDA Adverse Event
    Malfunction ·ACCURATE SURGICAL AND SCIENTIFIC INSTRUMENTS CORP.·Product code EMF·February 26, 2021

    BREAST RETRACTOR WITH FIBER OPTIC

    FDA Adverse Event
    ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP. (ASSI)·Product code GAD·January 18, 2012

    ASIM TENOTOMY SCISSORS

    FDA Adverse Event
    Injury ·ASSI - ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP·Product code LRW·June 30, 2010

    FOC158/75 FIBER OPTIC LIGHT CABLE 3.5MM X 2300MM

    FDA Adverse Event
    Malfunction ·ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP. (ASSI)·Product code FCW·February 7, 2024

    LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

    FDA Recall
    Open, Classified ·Linkbio Corp.·Product code QHE·March 12, 2026

    Tibial Array and Femoral Array. Model Number(s): 0150ARR00001 and 0150ARR00002. Manufactured by: MAKO Surgical, Corp. The devices are accessories used with MAKO's Tactile Guidance System (TGS). The Tactile Guidance System is intended to assist the surgeon in providing software defined spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures.

    FDA Recall
    Terminated ·Mako Surgical Corporation·Product code HAW·May 2, 2008

    Non-sterile Viscot Surgical Skin Markers Part Number 1437-100 Non-sterile Viscot Part Number 143-100 Surgical Skin Markers are pen-like devices intended to be used to write on the patient's skin, e.g., to outline surgical incision sites or mark anatomical sites for accurate blood pressure measurement; available in nonsterile configuration.

    FDA Recall
    Terminated ·Precision Dynamics Corporation·Product code FZZ·July 10, 2013

    Emergo Europe B.V.

    Authorized representative
    🇳🇱 Netherlands·900 Manufacturers·22100 Devices

    CMC Medical Devices & Drugs SL

    Authorized representative
    🇪🇸 Spain·698 Manufacturers·11260 Devices

    Shanghai International Holding Corp. GmbH(Europe)

    Authorized representative
    🇩🇪 Germany·637 Manufacturers·33064 Devices