BEUDAMED
    34 results · 30ms · Sources: EU EUDAMED, US FDA

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    ULTICARE SAFETY INSULIN SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GEN4 INTERACTIVE

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828173285·GEN4 INTERACTIVE

    Altus Spine Cervical Interbody Fusion System

    FDA UDI
    Altus Spine, LLC·00843210131177·Rasp, No Tab

    STEFAN BONE HOLDING FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896050716·STEFAN BONE HOLDING FORCEPS WITH SPEED LOCK CUR...

    GEN4 INTERACTIVE

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828190930·GEN4 INTERACTIVE

    GEN4 INTERACTIVE

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828166614·GEN4 INTERACTIVE

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193108179·HA PEEK EVOS Straight, ,11mmx9mmx 22mm , FLAT ...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694043342·Chin Plate 8mm with Screws, Sterile

    Monster® Screw System

    FDA UDI
    Paragon 28, Inc.·00889795040640·Over Drill, 3.0 x 110mm, Cannulated, AO

    HANKS' BALANCED SALT SOLUTION (HBSS) NO. 210-3011

    FDA 510(k)
    FDA Class 1 ·Hematology

    CONMED

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code LKF·January 5, 2012

    CONMED

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code LKF·January 5, 2012

    SELF ETCH BONDING PRIMER

    FDA 510(k)
    FDA Class 2 ·Dental

    FISHER & PAYKEL HEALTHCARE BUBBLE CPAP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VCARE VAGINAL-CERVICAL RETRACTOR-ELEVATOR

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code LKF·February 10, 2012

    BD ECLIPSE SMARTSLIP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·February 17, 2026

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 9, 2013

    ENDURANT II BIFURCATED STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·September 19, 2014

    ARCHITECT C4000 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·May 25, 2011

    BD PLASTIPACK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·November 10, 2021