BEUDAMED
    38 results · 22ms · Sources: EU EUDAMED, US FDA

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    STRYKER KNIFELIGHT

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

    Dornier MedTech

    FDA UDI
    Dornier MedTech GmbH·04049958001468·600 Micron Disposable Diode Laser Lightguide, 3...

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964062544·Endo Carry-On Procedure Kit

    V.A.T.S. DENNIS DISSECTING CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896003828·V.A.T.S. DENNIS DISSECTING CLAMP WITH RATCHET C...

    V.A.T.S. DENNIS DISSECTING CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921008840·V.A.T.S. DENNIS DISSECTING CLAMP WITH RATCHET C...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450178416·

    NITANIUM® ARCHWIRES

    FDA UDI
    Ortho Organizers, Inc.·00190707065683·.018 Upper Coated Nitanium® Pro Form™ Archwires

    Monoblock Tibial Trial UC Insert

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215043667·

    MAXCUT DIAMOND BURS (6/pk) MED 884-012

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D778100884121·MAXCUT DIAMOND BURS (6/pk) Shape: Pointed Cylin...

    TITANIUM COMPRESSION ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD PROBETEC ET MYCOBACTERIUM TUBERCULOSIS COMPLEX (CTB) CULTURE IDENTIFICATION ASSAY

    FDA 510(k)
    FDA Class 1 ·Microbiology

    INCLUSIVE MINI IMPLANT O-BALL 2.2 MMD X 13 MML

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 21, 2024

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·February 27, 2026

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013

    ONE TOUCH ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·August 6, 2008

    CONTOUR CURVED CUTTER STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 24, 2011

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·April 18, 2019

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 2, 2020

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 18, 2021

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·April 21, 2021