BEUDAMED
    18 results · 21ms · Sources: EU EUDAMED, US FDA

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    Mirus Ligating Clip, Mirus Ligating Clip Applier

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DEBAKEY FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896060333·DEBAKEY FORCEPS MICROSCOPIC ROUND HANDLE COUNTE...

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113998·HYDRO-DISSECT CANNULA VERTICAL 27GA

    N/A

    FDA UDI
    NORTHGATE TECHNOLOGIES INC.·00817183020721·CO2 Hose and DISS, Insufflation

    NA

    FDA UDI
    ZIMMER TRABECULAR METAL TECHNOLOGY INC.·00889024306288·

    Posterior Fusion Plate, HA Posterior Fusion Plate

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SMR GLENOSPHERE 36MM SMALL-R

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code KWS·December 3, 2020

    SYRINGE 3ML LL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·October 15, 2025

    TRUEMETRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·May 1, 2018

    ACCESS 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Other ·BECKMAN COULTER, INC.·Product code DHA·October 1, 2008

    INSYNC

    FDA Adverse Event
    Death ·MEDTRONIC S.A.·Product code DXY·August 10, 2011

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·July 1, 2013

    INBONE CANNULA FOOT BOTTOM

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY INC·Product code LXH·December 17, 2025

    INBONE DRILL 6MM STERILE

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY INC·Product code GFG·December 17, 2025

    ANSPACH***REF SP-4605-00***Arthroscopic Suture Anchor assembly with Suture Threader***Rx Only*** This device is intended to be used with Anspach Systems

    FDA Enforcement
    Class II ·Terminated·The Anspach Effort, Inc.·July 2, 2014

    Active Articulation E1. Intended for use with either primary or revision hip arthroplasty.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·June 12, 2013

    Medrad Continuum MR Infusion system- non-wireless system The MEDRAD Continuum MR Infusion System is designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prior to, during and immediately after the MR procedure functioning while either stationary or mobile. It is not intended to provide long-term patient care outside the MR environment. The system is to be used by trained medical staff, primarily critical care, emergency room and radiology nursing staff.

    FDA Enforcement
    Class II ·Terminated·Bayer Corp·June 11, 2014