BEUDAMED
    8 results · 20ms · 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.

    CONVERSE ALTAR RETRACTOR

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110645·COAXIAL IRR-ASP TIP STR W/SILICONE 0.4MM

    TRAY, SUTURE REMOVAL

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    SOFT SACK IV FLUID WARMER, THE FLOORMOUNT IV FLUID WARMER, THE PAK 2 IV WARMER AND THE THERMAL SAC PRESSURE INFUSER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·September 26, 2012

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·April 4, 2014

    HUDSON CORR-A-FLEX TUBING - 72"

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BYX·July 14, 2010

    Model Number U228, VISIONIST CRT-P EL MRI

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025