BEUDAMED
    27 results · 23ms · 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 ×

    AUTOLoader, and NOVA view with models: ALDR1000, AND NV2000

    FDA 510(k)
    FDA Class 2 ·Immunology

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690197096·Revision Knee Spiral Reamer- Hudson Short Flute...

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111026676·SKLAR STITCH SCISSOR ANG 5"

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100295·FRANKEL INFANT EYE SPECULUM

    Zimmer Persona Knee System

    FDA UDI
    Zimmer, Inc.·00889024508453·

    KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK

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

    CO2 monitoring line with and without in-line filter

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AFFIXUS HIP FRACTURE NAIL 125 DEG 9MM X 180MM

    FDA Adverse Event
    Injury ·BIOMET TRAUMA·Product code HSB·July 25, 2017

    CLEARLINK PACLITAXEL SETS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·February 2, 2024

    ASKU

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 6, 2026

    SEE H10

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 17, 2020

    ASKU

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 3, 2026

    ASKU

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 3, 2026

    DUO-VENT CLEARLINK LUER ACTIVATED VALVE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·July 12, 2023

    NI

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·May 23, 2017

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 8, 2013

    EON RECHARGEABLE IPG, 16-CHANNEL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 23, 2011

    POLYFLUX S CAPILLARY DIALYZER

    FDA Adverse Event
    Malfunction ·GAMBRO DIAYLZATOREN GMBH·Product code KDI·September 4, 2008

    NI

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·May 23, 2017

    TRUE METRIX

    FDA Adverse Event
    Injury ·TRIVIDIA HEALTH INC·Product code NBW·April 9, 2021