BEUDAMED
    33 results · 21ms · Sources: EU EUDAMED, US FDA

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    INSTANT-VIEW PHENCYCLIDINE (PCP) URINE DIP STRIP TEST

    FDA 510(k)
    FDA Unclassified ·Unknown

    Endo Carry-on Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964054189·Endo Carry-on Procedure Kit Includes Basin, Int...

    Armstrong

    FDA UDI
    MEDTRONIC XOMED, INC.·00681490028141·VENT TUBE 1010045 5PK ARMSTRG BEV STR 10

    Santis Pre Bent Rod 5.5mmx45mm

    FDA UDI
    Lanterna Medical Technologies GmbH·07640159550563·Santis Pre Bent Rod 5.5mmx45mm

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659173286·6.5 Cancellous Bone Shaft Screw, hex, _x000D_...

    SANTIS™ PRE BENT ROD 5.5mm X45mm -STERILE

    FDA UDI
    Lanterna Medical Technologies GmbH·07640159551683·SANTIS™ PRE BENT ROD 5.5mm X45mm -STERILE

    GMA 2.0 Pedicle Screw System

    FDA UDI
    GRAFTON MEDICAL ALLIANCE, INC.·00810021380230·PRE-BENT ROD, ø5.5 X 45

    Integrity-SI Fusion System

    FDA UDI
    Lincotek Medical LLC·B57112521010045D0·10 x 45 mm Anodized SI Implant

    6.5 Cancellous Bone Shaft Screw, hex, St.Steel, L 45/16 mm

    FDA UDI
    mahe medical gmbh·EMAH00100100450·6.5 Cancellous Bone Shaft Screw, hex, St.Ste...

    QUICK SET

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·October 30, 2025

    CYNOSURE PHOTOGENICA DL

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

    POSITUBE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    QUICK SET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 18, 2025

    MINIMED QUICK-SET

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·June 10, 2025

    SPEEDSTITCH SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code GAT·April 11, 2012

    AXSYM DIGOXIN III

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

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

    DUR MAR 10D LINER 28IDX52OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code LPH·February 28, 2011

    MINIMED QUICK-SET

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·June 6, 2025

    4F SINGLE MIDLINE MAX BARRIER KIT

    FDA Adverse Event
    Malfunction ·VYGON USA·Product code LJS·June 8, 2022