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

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    MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP3AX1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Strattice Reconstructive Tissue Matrix

    FDA UDI
    LIFECELL CORPORATION·M32820400020·Strattice Reconstructive Tissue Matrix, 20 x 40...

    Goode T-Tube®

    FDA UDI
    MEDTRONIC XOMED, INC.·00681490031035·VENT TUBE 1040002 10PK PR MOD T 1.27

    Goode T-Tube®

    FDA UDI
    MEDTRONIC XOMED, INC.·00763000039172·VENT TUBE 1040002 10PK PR MOD T 1.27

    Trilogy 200

    FDA UDI
    Respironics, Inc.·00606959022713·Garbin Plus Ventilator, International

    n/a

    FDA UDI
    Ortho Development Corporation·00822409073719·10/12 Collar Reamer MED

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221048844·3M™ Unitek™ Lingual Button, 20400-02, Curved Bo...

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481115165·F-Tx Attachment System, Narrow CrossFit (NC) Co...

    20GA Curved Laser Probe, SMA905

    FDA UDI
    Peregrine Surgical, Llc·00632307001673·20GA Curved Laser Probe, SMA905

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869634755·MOSS VRS Ti Locking Cap Star 27

    MAGNA 5000 PHASED ARRAY CTL SPINE COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    IMMULITE CK-MB, MODEL LKMB1 (100 TESTS), LKMB5 (500 TESTS); IMMULITE 2000 CK-MB, MODEL L2KMB2 (200 TESTS), L2KMB6 (600)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·ENDOLOGIX POWERLINK SYSTEM

    RESOLUTION CLIP

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code KOG·April 2, 2013

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORP·Product code LZG·March 25, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·May 6, 2008

    BD AUTOSHIELD DUO SAFETY PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·September 29, 2022

    BD AUTOSHIELD¿ DUO PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·October 31, 2022

    ConMed Laparoscopic Instrument: Curved ''Maryland'' Disposable Dissector, 5mm x 33cm length, REF/Product Code 60-6040-002. --- The product is distributed sterile in heat-sealed tray and labeled with an expiration date that pertains only to the sterility.

    FDA Recall
    Terminated ·Conmed Corporation·Product code GCJ·October 12, 2006

    UNKNOWN STRATTICE

    FDA Adverse Event
    Injury ·Product code FTM·July 12, 2022