BEUDAMED
    14 results · 21ms · 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 ×

    TRACH TIE, VENTILATOR TUBING HOLDER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    n/a

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994866691·CURETTE 2942016 PULL CURETTE5.5MM 90

    Ophthalmic Scissors

    FDA UDI
    KATENA PRODUCTS, INC.·00841668105177·TERRY MICRO CORNEAL SCISSORS RIGHT

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123014·K-WIRE - SINGLE TROCAR 2.0mm DIA x 150mm

    CAPRI

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DATASCOPE PROGUIDE CHRONIC DIALYSIS CATHETER

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

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024157415·

    DIRECT LATERAL INSTRUMENTS

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code LXH·August 25, 2025

    DIRECT LATERAL INSTRUMENTS

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·January 24, 2025

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code EZW·February 4, 2013

    PLMA DVC V11.51 1 R

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·November 9, 2010

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 5, 2014

    DIRECT LATERAL INSTRUMENTS

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·October 16, 2024

    DIRECT LATERAL INSTRUMENTS

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·March 4, 2025