BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    PENTEX BOVINE ALBUMIN 30% SOLUTION

    FDA 510(k)
    FDA Class 2 ·Hematology

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306835940·Stainless Steel, 3" Ultra Fine Mesh Strainer fo...

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code DSP·August 11, 1998

    SYNTHES 4.5 MM AND 6.5 MM HEADLESS COMPRESSION SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CEMEX SYSTEM GUN APPLICATION VERSION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OXF ANATOMIC BRG LT SM SIZE 5

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·May 8, 2014

    ON-Q SILVER SOAKER CATHETER

    FDA Adverse Event
    Injury ·I-FLOW, LLC·Product code BSO·October 18, 2012

    COMPRESSION ANASTOMOSIS RING (CAR 27)

    FDA Adverse Event
    Injury ·NITI SURGICAL SOLUTIONS LTD.·Product code FZP·August 10, 2010

    HLS Set Advanced, Model: BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Product Code/Part Number: 70105.2794 - Product Usage: These devices are used with the CARDIOHELP system in order to provide extracorporeal circulation for cardiac support and/or pulmonary support.

    FDA Recall
    Terminated ·Maquet Cardiovascular Us Sales, Llc·Product code DTZ·November 20, 2020

    HLS Set Advanced Model Name: BEQ-HLS 5050 USA; HLS Set Advanced 5.0, Product Code/Part Number: 70105.2797 - Product Usage: These devices are used with the CARDIOHELP system in order to provide extracorporeal circulation for cardiac support and/or pulmonary support.

    FDA Recall
    Terminated ·Maquet Cardiovascular Us Sales, Llc·Product code DTZ·November 20, 2020