BEUDAMED
    15 results · 30ms · 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.

    CLEANING BRUSH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RIWO-ART

    FDA UDI
    Richard Wolf GmbH·04055207022580·TROCAR TIP DULL SZ 12.7MM WL 164MM distal tip ...

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123052·K-WIRE - DOUBLE TROCAR 1.0mm DIA x 75mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150706·K-WIRE - SINGLE TROCAR 1.0mm DIA x 75mm

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867377134·GLENOID INSERTER/IMPACTOR, LARGE

    IVUS PLUS

    FDA 510(k)
    FDA Class 2 ·Radiology

    SEP 90

    FDA 510(k)
    FDA Class 2 ·Radiology

    GLENOID INSERTER/IMPACTOR, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 1, 2025

    GLENOID INSERTER/IMPACTOR, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·December 6, 2024

    GLENOID INSERTER/IMPACTOR, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 20, 2025

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·January 22, 2013

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    ANGLED REAMER, DRIVE SHAFT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·November 17, 2023

    ANGLED REAMER SLEEVE, 10°

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·November 17, 2023