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

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    NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110928·STERILIZING CASE SINGLE VR

    TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    LAMINATED KARAYA GUM WASHERS

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    GALAXY INTRAVASCULAR ULTRASOUND SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code IYO·January 17, 2013

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (STANDARD)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·December 8, 2010

    PRECISION SPECTRA®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 8, 2014

    BW Lasso 2515 ANV eco Variable Diagnostic EP Catheter, REF D134301 Diagnostic electrophysiology (EP) catheters are specially designed electrode catheters that transmit electrical impulses and can be positioned for endocardial recording or stimulation.

    FDA Enforcement
    Class II ·Terminated·Stryker Sustainability Solutions·January 30, 2019