BEUDAMED
    102 results · 28ms · Sources: EU EUDAMED, US FDA

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    Versana Premier; Versana Premier Lotus; LOGIQ F

    FDA 510(k)
    FDA Class 2 ·Radiology

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·24026704515251·

    NA

    FDA UDI
    Medos International Sàrl·10886705028764·HD EP Arthroscope/Sinuscope compatible with Sto...

    Introcan Safety ® 2

    FDA UDI
    B. BRAUN MEDICAL INC.·04046955745906·INTROCAN SAFETY 2 W PUR 22GX25MM - US

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180159785·6.5MM, NATHANSON RETRACTOR-COOK STYLE, LARGE, 75MM

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776208837·Nathanson Retractor cook style large

    Perfect Fit

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377021336·Perfect Fit™II R/S Interface Module Cable, Ches...

    Comfortear™

    FDA UDI
    MICROSPECIALITIES, INC.·10810003223576·Comfortear™ Punctum Plugs are packaged sterile ...

    Symmetry Charnley

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482061060·Symmetry® Retractor, Charnley Blade, Long Round...

    SpineFab Vertebral Body Replacement (VBR) System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACHTUNG TD-4207, CLEVER CHEK TD-4209, CLEVER CHEK TD-4222

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PFC SIGMA/OV/DOME PAT 3PEG.35

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·September 22, 2005

    PFC SIGMARP CV TB/IN S3 10.0

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·September 22, 2005

    PHILOS DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.,·Product code DXY·November 17, 2005

    *

    FDA Adverse Event
    Injury ·JOHNSON AND JOHNSON DEPUY SPINE, INC·Product code KWQ·September 22, 2005

    DUAL LUMEN INSERTION TRAY

    FDA Adverse Event
    TYCO/KENDALL HEALTHCARE·Product code LJS·November 15, 2005

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·October 28, 2005

    VITALITY DS

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·February 8, 2007

    SYNCHROMED EL

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code LKK·June 23, 2005

    NATURAL-KNEE II SYSTEM CONGRUENT TIBIAL INSERT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·November 18, 2005