BEUDAMED
    73 results · 25ms · Sources: EU EUDAMED, US FDA

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    GE MARQUETTE CLINICAL INFORMATION CENTER, GE MARQUETTE CIC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001112·artVeneer life upper anteriors, IXL, A35

    n/a

    FDA UDI
    Ortho Development Corporation·00822409090631·Reamer 11-12

    Masel

    FDA UDI
    Ortho Organizers, Inc.·00190707007829·CHEEK RETRACTOR INTRAORAL MEDIUM

    Fuji Cervical Plate System

    FDA UDI
    Altus Spine, LLC·00843210121802·Twist Drill, 4mm x 12mm

    Scanlan® TIP-GUARD™ instrument protectors - Endoscopic

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159001822·Scanlan® TIP-GUARD™ instrument protectors - End...

    PRCT2

    FDA UDI
    FX SOLUTIONS·03701037307656·PRCT II TRIAL PLATE LEFT 12 HOLES

    Duo Lumbar Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7401001112·Duo Straight Inserter Fork

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918184449·Femoral_Angiography_Drape_with dual windows_381...

    DIGITAL INTEGRATION SYSTEM, DIS2000

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACUCAM CONCEPT IV, MODELS A1222B, A1223B, A1221B, A1121B, A1222C, A10402, A10403, A10401

    FDA 510(k)
    FDA Class 1 ·Dental

    ZIMMER NEXGEN ARTICUL

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·May 1, 2017

    VANGUARD PFR FEMORAL LT SM

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRR·May 17, 2018

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013

    POLIGRIP

    FDA Adverse Event
    Other ·GLAXOSMITHKLINE·Product code KOL·February 16, 2011

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·February 14, 2008

    STERNALOCK BLU SYSTEM BLADE, STERNALOCK POWERDRIVER

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code OYC·May 22, 2018

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code OYC·April 5, 2017

    RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019