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

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    Berkeley VC-10 Vacuum Curettage System

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    VC10 PUMP, 115V

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code HHK·January 2, 2025

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741714400·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674171440060·

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169596009·TRIAL 2171440 O25 IB 20MM 6 DEG 14X40

    NC/RC Variobase Coping,screw-retained abutment

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600381501·

    BioCosmetic®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR21714401·BioCosmetic arches coated Straight-Arch-F. max....

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100752·FLIERINGA FIXATION RING 14MM

    Ambler Value Line

    FDA UDI
    AMBLER SURGICAL CORP.·00190660214203·Deaver retractor, 12'' long x 1'' wide blade, f...

    ENCORE TONGUE SUSPENSION SYSTEM ENCORE REMOVAL-TITRATION KIT

    FDA 510(k)
    FDA Class 2 ·Dental

    GMD UNIVERSAL URINARY INCONTINENCE SLING, MODEL 1012

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

    INCORPORATE

    FDA UDI
    SPINAL ELEMENTS·00840606151955·17 X 14 CERVICAL TRIALS 40MM 0° LORDOSIS

    INCORPORATE

    FDA UDI
    SPINAL ELEMENTS·00840606152143·17 X 14 CERVICAL TRIALS 40MM 10° LORDOSIS

    REFOBACIN BONE CEMENT R 1X40-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 30, 2026

    REFOBACIN BONE CEMENT R 1X40-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·February 24, 2026

    OPTIPAC 80 REFOB PLUS BONE CMT-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2026

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 12, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·October 14, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013

    CONTINUOUS NERVE BLOCK KIT

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code CAZ·June 30, 2011