BEUDAMED
    16 results · 21ms · Sources: EU EUDAMED, US FDA

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    CRONEX QUANTA SR300 INTENSIFYING SCREEN

    FDA 510(k)
    FDA Class 1 ·Radiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04046114410669·***DISC***MEDI BIG ARM BUTLER

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517382375·CoRoent XLR Curette, Right Angled

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950016464·SYRINGE TIP AIR 4-1/2" 11CM 2.2MM OPENING

    WINCH KYPHOPLASTY KIT 15MM

    FDA Adverse Event
    Malfunction ·G21 S.R.L.·Product code NDN·June 21, 2024

    i-ED COIL

    FDA UDI
    KANEKA CORPORATION·04540778176447·The i-ED COIL is used for vascular embolization...

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746099076·DB BKT MASTER LL CUSP 022 T-11 A+7 R2M

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690192978·Femoral Locating Device Bushing 3 deg

    Illumena 150mL Linden Luer Syringe with Handi-Fil Straw (p/n 900103) & Illumena 150mL Regular Luer Syringe with Handi-Fil (p/n 900101), Made in Mexico, Liebel-Flarsheim Company, Cincinnati, OH The Liebel Flarsheim Illumena 150mL Syringes with Handi-Fil Straw are designed for use with the Illumena Injector System. The Angiomat Illumena is designed to inject a radiopaque contrast medium into the vascular system for Angiographic or CT procedures.

    FDA Recall
    Terminated ·Mallinckrodt Inc·Product code IZQ·October 11, 2011

    Angiomat Illumena Syringe, 150mL Linden Luer Syringe with Handi-Fil Straw (p/n 900103), in a sealed molded plastic tray. The Liebel Flarsheim Illumena 150 mL Linden Luer Syringe with Handi-Fil Straw is designed for use with the Illumena Injector System. The Angiomat Illumena is designed to inject a radiopaque contrast medium into the vascular system for Angiographic or CT procedures as prescribed by qualified health care professionals.

    FDA Recall
    Terminated ·Mallinckrodt Inc·Product code IZQ·May 20, 2011

    100KGY E-POLY ACETABULAR LINERS- ADDITIONAL PROFILES: +3 MAXROM AND +3 HI-WALL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AVL OPTI R ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·February 10, 2015

    LAMITRODE TRIPOLE 16

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 28, 2014

    LIGACLIP** ENDOSCOPIC CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·January 7, 2013

    HEARTSTRING PROXIMAL SEAL, 4.5 MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·October 22, 2010