BEUDAMED
    15 results · 20ms · Sources: EU EUDAMED, US FDA

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    Venue Go

    FDA 510(k)
    FDA Class 2 ·Radiology

    Philips

    FDA UDI
    Sbo Hearing A/S·05714464052462·HEARLINK 9030 FW 1.3.0

    Reddick Cholangiogram Catheter

    FDA UDI
    Lemaitre Vascular, Inc.·00840663106912·Reddick Cholangiogram Stiffer Catheter with Nee...

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00841785113420·

    Reddick Cholangiogram Catheter

    FDA UDI
    Lemaitre Vascular, Inc.·00840663107278·Reddick Cholangiogram Stiffer Catheter with Nee...

    Trial BiPolar Head

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215045586·

    KANGLI PEDICLE SCREW SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRECISION VPS IMPRESSION MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    CELL-DYN WBC REAGENT A

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·November 24, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

    ENERGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 22, 2013

    LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (eIFU) REF # e2400-53

    FDA Recall
    Terminated ·LeMaitre Vascular, Inc.·Product code DQO·February 7, 2017

    LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (eIFU) REF # e2400-53

    FDA Enforcement
    Class II ·Terminated·LeMaitre Vascular, Inc.·March 22, 2017

    REDDICK CHOLANGIOGRAM CATHETER

    FDA Adverse Event
    Malfunction ·LEMAITRE VASCULAR INC·Product code GBZ·October 1, 2012

    Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020

    FDA Enforcement
    Class II ·Terminated·Cardinal Health 200, LLC·February 26, 2020