BEUDAMED
    23 results · 22ms · Sources: EU EUDAMED, US FDA

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    Zsquare ENT-Flex Endoscope

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040188200·Zirlux Nightguard & Splint Print Resin - Flexible

    KeyPrint

    FDA UDI
    Keystone Industries·H66842200041·KeySplint Hard 1 kg

    ACRY PRINT RU-004 Denture HI

    FDA UDI
    pro3dure medical GmbH·EPRC0220004·ACRY PRINT RU-004 Denture HI 1000g Orange-Pink

    PMT® Halo Systems

    FDA UDI
    PMT CORPORATION·00650551122708·HALO, 1220-5 VEST SMALL, LAMBSWOOL LINER, 1211-...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694007382·1.1mm Pilot Drill, 4mm Stop, J-Latch

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989044256·CROWN-PERM LL 4 1ST MOLAR SST PK/5

    TriplePlay

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377021923·Interface Cable, Snore, Keyhole

    Pulmonary Stent

    FDA Pre-Market Approval
    FDA Class 3 ·PALMAZ MULLINS XD Pulmonary Stent

    (MULTIPLE) DIGITAL THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CLINDATALINK VERSION 1.0 FOR SPIROMETRY

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Pulmonary Stent

    FDA Pre-Market Approval
    FDA Class 3 ·PALMAZ MULLINS XD Pulmonary Stent

    Pulmonary Stent

    FDA Pre-Market Approval
    FDA Class 3 ·PALMAZ MULLINS XD Pulmonary Stent

    ONE TOUCH BASIC ENHANCED

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code CFR·February 3, 2004

    ECHO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·November 6, 2008

    HCG COMBO DEVICE SP BRAND RAPID TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHI·July 13, 2011

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·July 11, 2013

    INSPIRA SMOOTH COHESIVE SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·May 11, 2023

    PERSONA 2 PEG POROUS TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code MBH·November 17, 2015

    PERSONA TIBIA CEMENTED 5 DEGREE STEMMED RIGHT SIZE C

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code MBH·December 22, 2025