BEUDAMED
    70 results · 23ms · Sources: EU EUDAMED, US FDA

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    CardioChek Plus Test System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    XENMATRIX

    FDA UDI
    Davol Inc.·00801741128998·XenMatrix AB Surgical Graft, 15 cm x 30 cm

    BONE SCREW, CORTICAL

    FDA UDI
    Biomet Orthopedics, LLC·00887868004681·

    ProLift Trial

    FDA UDI
    Life Spine, Inc.·00190837088606·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694046916·PrimaLIF LLIF PEEK Implant, 15mm X 18mm X 30mm,...

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00842962103395·UTERINE INJECTOR, 2mm, STERILE, BOX OF 12

    MONARC + SUBFASCIAL HAMMOCK, MODEL 72404193; MONARC C SUBFASCIAL HAMMOCK, MODEL 72404195.

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

    EVOLUTION DUODENAL STENT SYSTEM, MODEL EVO-22-27-6-D, EVO-22-27-9-D, EVP-22-27-12-D

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

    Canaveral®

    FDA UDI
    FLOSPINE LLC·B183115150300·Reduction Monoaxial Screw, 10.5mm x 30mm

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00842962101469·UTERINE INJECTOR, 2mm, STERILE

    CUP: VERSAFITCUP CC TRIO 01.26.45.1156 ACETABULAR SHELL CC TRIO NO-HOLE Ø 56

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·March 16, 2023

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 17, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·December 28, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·October 12, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·August 9, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 7, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 6, 2011

    CARPENTIER-EDWARDS PHYSIO ANNULOPLASTY RING

    FDA Adverse Event
    Other ·EDWARDS LIFESCIENCES·Product code KRH·September 5, 2008