BEUDAMED
    23 results · 23ms · Sources: EU EUDAMED, US FDA

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    CD HORIZON SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·December 7, 2018

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NKB·November 30, 2020

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NKB·September 8, 2020

    NexxZr™ T / D-100-10-NT-C200-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271113214·

    R & D BATTERIES, INC.

    FDA registration
    R & D BATTERIES, INC.·20 products·🇺🇸 United States

    WaveForm TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981233303·Interbody, 11mm x 32mm x 11mm, 10 Deg, 3D

    WaveForm TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981288785·Interbody, 11mm x 32mm x 11mm, 10 Deg, 3D

    Aileron Expandable Posterior Fusion System

    FDA UDI
    Life Spine, Inc.·00190837000134·

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981204600·Trial, 11mm x 32mm x 11mm, 10 Deg

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981190453·Interbody, 11mm x 32mm x 11mm, 10 Deg

    RAVINE Lateral Access System

    FDA UDI
    VB Spine LLC·10888857560987·A/P Lateral Access Blade Size 13x170 mm

    MEDICAL MAGNETIC TAPE RECORDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACUSON CV70 CARDIOVASCULAR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523184149·L CR E-CIMA Vitamin E Ultracongruent Tibial Ins...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523184385·L Ultracongruent Tibial Insert Trial Sz A 11mm

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·June 16, 2011

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024