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

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    LIQUOGUARD CSF LIQUOGUARD CSF TUBING SET (1500MM) LIQUOGUARD CSF TUBING SET (2000MM) SAFETY CUSHION FOR TUBING SET ATTAC

    FDA 510(k)
    FDA Class 2 ·Neurology

    NOVO Health Services, LLC

    FDA UDI
    NOVO HEALTH SERVICES, LLC·00812564032201·2 GOWN BASIC PACK

    ArgenZ Anterior 95x16

    FDA UDI
    ARGEN CORPORATION, THE·D818121248·Dental porcelain/ceramic restoration kit

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·10884450390334·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970386·

    ICASE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    NON-STERILE, POWDER-FREE NITRILE EXAMINATION GLOVES (ORIGINAL BLUE, COBALT BLUE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    IDENTITY XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.CRMD·Product code DXY·January 13, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013

    ASR ACETABULAR CUPS 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 1, 2011

    UNK HIP FEMORAL STEM ACTIS

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code LPH·October 9, 2023

    UNK HIP FEMORAL STEM ACTIS

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code LPH·October 9, 2023

    UNK HIP FEMORAL STEM ACTIS

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code LPH·October 9, 2023

    UNK HIP FEMORAL STEM ACTIS

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code LPH·October 9, 2023

    UNK HIP FEMORAL STEM ACTIS

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code LPH·October 9, 2023