BEUDAMED
    13 results · 21ms · 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 ×

    AuST Steerable Sheath

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LCP

    FDA UDI
    Synthes GmbH·10886982167941·4.5MM LCP® PROXIMAL FEMUR PLATE 6 HOLES/211MM-LEFT

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112755·BARRON VACUUM PUNCH 7.5MM

    ELMED INCORPORATED

    FDA UDI
    ELMED INCORPORATED·00198506074868·FLAT OSTEOTOME; 20MM X 7-3/4"

    NA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295122760·FLAT OSTEOTOME 20mm

    DECISIO HEALTH PATIENT DASHBOARD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Plasmage System

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

    ACTICON NEOSPHINCTER

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code EZY·August 26, 2013

    BD LUER-LOK¿ TIP SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·April 7, 2023

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 10, 2014

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·September 9, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013

    PUMP MMT-1780KPK 670G PATHWAY BLACK MG

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 25, 2023