BEUDAMED
    935 results · 25ms · Sources: EU EUDAMED, US FDA

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    BeneHold Surgical Incise Drape with CHG antimicrobial

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699427·GENUMEDI SILVER SIZE VIII

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112779·BARRON VACUUM PUNCH 8.0MM

    24M - Salt River Project-21 - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588022017·24M - Salt River Project-21 - Metal

    VISICOIL MR

    FDA UDI
    Izi Medical Products, LLC·EIBASNMR03502022080·0.35mm x 2.0cm VISICOIL MR Platinum loaded into...

    VISICOIL MR

    FDA UDI
    Izi Medical Products, LLC·B887SNMR03502022080·0.35mm x 2.0cm VISICOIL MR Platinum loaded into...

    Agape Warming Personal Lubricant

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

    NANOGEN

    FDA 510(k)
    FDA Class 2 ·Dental

    670G INSULIN PUMP MMT-1780KL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·September 12, 2022

    PLUM A+/A+3 (V 11.X & 13.X)

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FRN·July 13, 2022

    640G INSULIN PUMP MMT-1712K

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·January 14, 2023

    COVID-19 AT HOME TEST

    FDA Adverse Event
    Malfunction ·SD BIOSENSOR, INC.·Product code QKP·May 3, 2022

    INFUSOMAT SPACE

    FDA Adverse Event
    Malfunction ·B.BRAUN MELSUNGEN AG·Product code FRN·September 1, 2022

    SYRINGE 10ML SALINE XS

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code FMF·April 27, 2020

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·October 16, 2008

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 5, 2011

    AF531 FULL FACE MASK

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code MNS·June 28, 2013

    BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·September 14, 2022

    CARDIOHELP

    FDA Adverse Event
    Death ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·August 24, 2022

    BD ALARIS SMARTSITE EXTENSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·January 10, 2022