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

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    ASAP MUITISCOPE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772813148·GENUMEDI PRO SILVER SIZE I

    CRYO.S

    FDA UDI
    Greiner Bio - One GmbH·14039943000016·

    ArgenZ Anterior 95x14 #1

    FDA UDI
    ARGEN CORPORATION, THE·D818121261·Dental porcelain/ceramic restoration kit

    SoloPace Fusion Sterile Pack

    FDA UDI
    SOLO PACE INC.·00850056280044·

    CORNEAL TREPHINE BLADE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896012929·CORNEAL TREPHINE BLADE

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383505826·Gutta Percha Points is used to root canal filin...

    CATHETER REPAIR KIT WITH REPLACEMENT CONNECTOR, MODEL 5587000

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SEEDNET SYSTEM AND SEEDNETGOLD SYSTEM, MODELS GP6T5, GP5T5, GP5T3, HP5T5 & HP5T3

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

    NV GXL LINR, NTRL, 36MM ID, GROUP 4 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·May 24, 2024

    OT VERIO IQ METER

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

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·September 22, 2014

    ASR ACETABULAR CUPS 50

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