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

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    Impla-NX (Model: ISE-270M)

    FDA 510(k)
    FDA Class 1 ·Dental

    Waterlase Laser Tips

    FDA UDI
    Biolase, Inc.·00647529002230·A single-use fiberoptic accessory intended for ...

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613153152842·STRAIGHT INSERT F. BONE GRASPING FORCEPS

    36M - Black & Veach - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588011820·36M - Black & Veach - Metal

    LIPOSUCTION CANNULA

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B0992011920·LIPOSUCTION CANNULA 1X2 TOTEM STYLE

    SELF ADHERING NAVIGUS GUIDE

    FDA 510(k)
    FDA Class 2 ·Neurology

    QACA IGG/IGM ELISA KIT HRP

    FDA 510(k)
    FDA Class 2 ·Immunology

    TROJAN NIRVANA COLLECTION LUBRICATED CONDOMS

    FDA Adverse Event
    Injury ·CHURCH & DWIGHT CO., INC.·Product code HIS·June 24, 2020

    OT VERIO FLEX METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE GMBH·Product code NBW·August 6, 2019

    GORE-TEX CARDIOVASCULAR PATCH

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DXZ·June 25, 2013

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·March 21, 2023

    CRYOFLEX

    FDA Adverse Event
    Injury ·MEDTRONIC ATS MEDICAL·Product code OCL·December 20, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 27, 2014

    HERCULES 3 STAGE BALLOON ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC.·Product code KNQ·July 29, 2011

    UNKNOWN DEPUY FEMORAL HEAD

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code KWY·July 2, 2013

    GORE-TEX SUTURE

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES,INC·Product code GAW·April 26, 2013

    GORE-TEX SUTURE

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code GAW·April 26, 2013

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·January 20, 2023

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·Product code HRS·November 6, 2017

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 17, 2017