BEUDAMED
    29 results · 20ms · Sources: EU EUDAMED, US FDA

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    INSTANT-VIEW MORPHINE (2000) URINE CASSETTE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Avitene

    FDA UDI
    Davol Inc.·00801741010453·Avitene Non-Woven Web, 35 mm x 35 mm x 1 mm

    PUMA-G System™

    FDA UDI
    Coaptech, Inc.·10860312001532·External Magnet in Case

    AccuSert

    FDA UDI
    EMED TECHNOLOGIES CORPORATION·00817708022988·SAF-SUB-Q Needle Inserter

    Santis Pre Bent Rod 5.5mmx80mm

    FDA UDI
    Lanterna Medical Technologies GmbH·07640159550631·Santis Pre Bent Rod 5.5mmx80mm

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C30430100800·PEEK PLIF Spacer, 30 x 10 x 8mm, 0 deg

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659173385·6.5 Cancellous Bone Shaft Screw, hex, _x000D_...

    SANTIS™ PRE BENT ROD 5.5mm X80mm -STERILE

    FDA UDI
    Lanterna Medical Technologies GmbH·07640159551751·SANTIS™ PRE BENT ROD 5.5mm X80mm -STERILE

    10 x 80mm Anodized SI Implant

    FDA UDI
    Osteocentric Technologies, Inc.·00810097800144·10 x 80mm Anodized SI Implant

    Integrity-SI Fusion System

    FDA UDI
    Lincotek Medical LLC·B57112521010080D0·10 x 80 mm Anodized SI Implant

    Caplugs/Evergreen

    FDA UDI
    CAPlugs·00810044201123·10 mL Sterile Transport Vials with Caps

    GMA 2.0 Pedicle Screw System

    FDA UDI
    GRAFTON MEDICAL ALLIANCE, INC.·00810021380285·PRE-BENT ROD, ø5.5 X 80

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C31430100800·Titanium PLIF Spacer, 30 x 10 x 8mm, 0 deg

    6.5 Cancellous Bone Shaft Screw, hex, St.Steel, L 80/16 mm

    FDA UDI
    mahe medical gmbh·EMAH00100100800·6.5 Cancellous Bone Shaft Screw, hex, St.Ste...

    SPINE SYSTEM EVOLUTION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ASNIS III CANNULATED SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYRINGE 1ML LS SP120

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·September 8, 2021

    SEE H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 15, 2011

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007