BEUDAMED
    119 results · 24ms · Sources: EU EUDAMED, US FDA

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    CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM

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

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040008478·Zirlux 16+ D2 89x17x16

    S NEEDLE

    FDA UDI
    asia-med GmbH·04251282512408·asia-med s-needle J-Type 3040 Place N' Press: c...

    S NEEDLE

    FDA UDI
    asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282505417·asia-med s-needle J-Type 3040 Place N' Press: c...

    FOSTER GRANT

    FDA UDI
    FGX INTERNATIONAL INC.·00193033369548·

    Integrity-SI Fusion System

    FDA UDI
    Lincotek Medical LLC·B57112521012056D0·12 x 55 mm SI Implant with HA Coating

    MICRUS MICROCOIL DELIVERY SYSTEM, MDS03

    FDA 510(k)
    FDA Class 2 ·Neurology

    UTERINE MANIPULATOR INJECTOR CANNULA, STERILE, MODEL R 57-450

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BD PLASTIPAK¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·January 19, 2023

    ACCU-CHEK D-TRONPLUS

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·March 20, 2013

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·February 28, 2011

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 14, 2007

    BD PLASTIPAK ¿ - 3-PIECE SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 5, 2023

    ACCESS 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code MMI·July 6, 2012

    PRESIDIO 10 - CERECYTE MICROCOIL

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code HCG·June 9, 2016

    PRESIDIO 18 - CERECYTE MICROCOIL

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code HCG·June 9, 2016

    Enpath Lead Adapters, pacemaker lead adapter. Affects: 5 mm Bipolar, Model 501205; 6 mm Unipolar, Model 501204; 3.2 mm Low-Profile Bipolar Models 501206 and 501214. All labeled Sterile, EO, mail: Enpath Medical, Inc. Lead Technologies Division, Minneapolis, MN 55439 USA.

    FDA Recall
    Terminated ·Enpath Medical, Inc·Product code DTB·July 18, 2006

    da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12

    FDA Recall
    Open, Classified ·Intuitive Surgical, Inc.·Product code NAY·June 12, 2023

    da Vinci Xi EndoWrist Stapler 45 Reload Green, Model 48445G-03, 12 reloads/box.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code GDW·April 23, 2018

    da Vinci Xi EndoWrist Stapler 45 Reload Blue, Model 48645B-03, 12 reloads/box.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code GDW·April 23, 2018