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

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    SPAZZ

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517594891·CoRoent Large MP Ti, 8x9x23mm 0°

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526743601·LEVAMED ANKLE SUPPORT SAND III

    60mL Medallion® Syringe

    FDA UDI
    Merit Medical Systems, Inc.·00884450397480·

    Kalitec Special

    FDA UDI
    Kalitec Direct LLC·B073DRK0100230·SNII Awl Tap, 7.50mm

    Matira

    FDA UDI
    Kalitec Direct LLC·B07307K0100230·Assembly, Caddie, 4L Plates, Hinged

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0100230·Caddie, Lid, Rods, Adjustable Cross Links, and ...

    LINKMAX

    FDA 510(k)
    FDA Class 2 ·Dental

    BIOCURVE SOFT (METHAFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014

    PRISMAFLEX

    FDA Adverse Event
    Death ·GAMBRO LUNDIA AB·Product code KDI·April 11, 2014

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·November 2, 2012

    APTIMA HPV SCREENING ASSAY

    FDA Adverse Event
    Injury ·HOLOGIC, INC.·Product code OYB·May 23, 2025

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 15, 2012

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·December 23, 2013

    LINA LOOP

    FDA Adverse Event
    Injury ·LINA MEDICAL POLSKA SP. Z.O.O·Product code KNF·January 19, 2010

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    DEPUY INTERNATIONAL·Product code KXA·March 19, 2013

    RIATA PASSIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008

    APTIMA COMBO 2 ASSAY

    FDA Adverse Event
    Injury ·HOLOGIC, INC.·Product code LSL·June 20, 2025

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014