BEUDAMED
    10 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.
    Filters Regulation: Us FDA ×

    GREINER VACUETTE BLOOD COLLECTION TUBE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020

    PEEK Corpectomy

    FDA UDI
    Nuvasive, Inc.·00887517623263·PEEK Corp Core, Ø12x36mm

    TRIOBEAD-125 DIAGNOSTIC KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ALCON MULTI-PURPOSE SOLUTION

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SPIROPERFECT

    FDA Adverse Event
    Malfunction ·MEDIKRO OY·Product code BZG·August 11, 2023

    G7 NEUTRAL E1 LINER 36MM D

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·June 5, 2020

    ELECTRIC DERMATOME HANDPIECE

    FDA Adverse Event
    Malfunction ·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code GFD·February 1, 2013

    CAPSURE EPI

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·January 26, 2011

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 31, 2014