BEUDAMED
    20 results · 23ms · Sources: EU EUDAMED, US FDA

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    ELITech Clinical Systems CALCIUM ARSENAZO

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    New Image

    FDA UDI
    HOLLISTER INCORPORATED·00610075073030·2-Piece Ostomy Skin Barrier, CeraPlus

    Nautilus Spinal System

    FDA UDI
    Life Spine, Inc.·00190837054922·Nautilus Deflection Beam Handle

    VARIANT

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SPO1511130·Smooth Fixation Pin, ø3mm x 130mm

    QUANTA SYSTEM ETRNA GIOVINEZZA

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

    GUARDIAN II NC HEMOSTASIS VALVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Trulink

    FDA UDI
    STATCORP MEDICAL·10841522128561·BP CUFF,TL SOFT,1T,INFANT,8-14CM,HP,5/BG

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007624·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007631·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007662·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007648·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007679·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007655·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    ILAB? POLARIS MULTI-MODALITY GUIDANCE SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·May 14, 2026

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·July 21, 2016

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

    PERPOS FUSION FACET PREP KIT

    FDA Adverse Event
    Malfunction ·INTERVENTIONAL SPINE, INC.·Product code HTW·June 20, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 9, 2008

    L CONNECTOR C90J

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code LHI·March 10, 2020

    Medical Linear Accelerator

    FDA Enforcement
    Class II ·Terminated·Elekta, Inc.·September 14, 2016