BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    MARKSMAN ARTERIAL BLOOD GAS SYRINGE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112359·SURG-I-BAND PURPLE GLOW

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112328·SURG-I-BAND GREEN

    PROSTEP™ TBI™ (Tailors Bunion Implant) System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWDERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    UNKNOWN RIGHT HIP STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·January 4, 2013

    EON MINI RECHARGEABLE IPG

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·November 23, 2010

    PROMOTE RF CRT-D

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·July 2, 2014