BEUDAMED
    27 results · 24ms · Sources: EU EUDAMED, US FDA

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    VECTOR

    FDA 510(k)
    FDA Class 2 ·Dental

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092002122·artVeneer life upper posteriors, L, C4

    SCANLAN®

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159018127·Vascular Clamp 25 mm Jaw

    BetaForce

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730022103·Beta3 Euro Upper 21x25 10 archwires per pack

    Metal Custom Rx

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746102462·BRACKET WIDE TWIN 022 TQ=25 A=0 R=0 PROFILE=STD...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197173674·Blakesley Forceps Fig. 2 Ø4.2mm...

    HEMOSTAT KELLY 8-3/4" SLIGHT CURVE

    FDA UDI
    W.H. Holden, Inc.·D928140021220·

    COLLAGRAFT STRIP BONE GRAFT MATRIX (FOR USE AS A BONE FILLER), MODEL 1X,3X,6X (1,3 OR 6 STRIPS PER BOX)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROLENE SOFT (POLYPROPYLENE), NONABSORBABALE SYNTHETIC SURGICAL MESH

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

    OBTAPE TRANSOBTURATOR SLING

    FDA Adverse Event
    Injury ·MENTOR WORLDWIDE LLC·Product code FTL·October 16, 2012

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE CR SIZE 3/12 MM L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·June 5, 2024

    2520274-2013-04648

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code LRN·August 27, 2013

    OMEGA21 EXPANSIVE SCREW 7X35MM

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code MNI·November 22, 2013

    2520274-2013-10213

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code MNI·February 11, 2013

    PHASEAL INFUSION ADAPTER

    FDA Adverse Event
    Malfunction ·CARMEL PHARMA AB·Product code LHI·February 1, 2011

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 20, 2008

    CATALYS SYSTEM

    FDA Adverse Event
    Malfunction ·AMO MANUFACTURING USA, LLC·Product code OOE·August 15, 2024

    TECNIS SIMPLICITY

    FDA Adverse Event
    Malfunction ·AMO MANUFACTURING NETHERLANDS·Product code MFK·August 5, 2025

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·August 2, 2011

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 30, 2023