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

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    Bone Sonometer

    FDA Pre-Market Approval
    FDA Class 2 ·THE SUNLIGHT OMNISENSE(TM) ULTRASOUND BONE SONOMETER

    Bone Sonometer

    FDA Pre-Market Approval
    FDA Class 2 ·OMNISENSE 7000S ULTRASOUND BONE SONOMETER

    Bone Sonometer

    FDA Pre-Market Approval
    FDA Class 2 ·SUNLIGHT OMNISENSE ULTRASOUND BONE SONOMETER

    Bone Sonometer

    FDA Pre-Market Approval
    FDA Class 2 ·SUNLIGHT OMNISENSE 7000S

    Bone Sonometer

    FDA Pre-Market Approval
    FDA Class 2 ·SUNLIGHT OMNISENSE BONE SONOMETER

    Bone Sonometer

    FDA Pre-Market Approval
    FDA Class 2 ·SUNLIGHT OMNISENSE 7000S ULTRASOUND BONE SONOMETER

    Bone Sonometer

    FDA Pre-Market Approval
    FDA Class 2 ·OMNISENSE 7000S ULTRASOUND BONE SONOMETER

    NA

    FDA UDI
    Richard Wolf GmbH·04055207045091·AMNIOSCOPE TUBE ID 16.9MM OD 20/27MM for child...

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377080509·RELINE C Holder, Rod-Rod Connector

    Copper Ni-Ti - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989086133·COPPER NITI 35 BAF 19X25 UP LG PK10 W/STOPS

    Uni-Patch

    FDA UDI
    Cardinal Health 200, LLC·20192253045540·Uni-Patch™ Conductive Gel Pad

    Uni-Patch

    FDA UDI
    Cardinal Health, Inc.·10884521171381·Conductive Gel Pads

    Pro-Retractor Horizontal Solid Bar

    FDA UDI
    KOROS U.S.A., INC.·10840199542281·Pro-Retractor Horizontal Solid Bar 1"

    NEXGEN FEMORAL COMPONENT OPTION FOR CEMENTED USE ONLY SIZE E LEFT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021

    PERSONA ARTICULAR SURFACE WITH HINGE POST EXTENSION SIZE E 20 MM HEIGHT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021

    PERSONA ARTICULAR SURFACE WITH SEGMENTAL HINGE POST SIZE E 20 MM HEIGHT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021

    RF

    FDA 510(k)
    FDA Class 2 ·Immunology

    System, Test, Tumor Marker, For Detection Of Bladder Cancer

    FDA Pre-Market Approval
    FDA Class 3 ·NMP22 BladderChek Test

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK(R) P2 SYSTEM

    RIGHT SIZE E CEMENTED OPTION FEMORAL COMPONENT FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2023