BEUDAMED
    11 results · 27ms · 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.

    RETRACTOR, SURGICAL

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

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209108435·KIT, MARCH IFAK with CG (vac) - CUSTOM

    Ophthalmic Forceps

    FDA UDI
    KATENA PRODUCTS, INC.·00841668106273·KELMAN-MCPHERSON FORCEPS 1X2 TEETH

    Expression MR400 MRI Patient Monitoring System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRU-SWAB STOCOCK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 5, 2014

    SPINBRUSH PRO WHITENING POWERED TOOTHBRUSH

    FDA Adverse Event
    Malfunction ·CHURCH & DWIGHT CO., INC.·Product code JEQ·November 13, 2012

    PENTA LEAD

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 29, 2010

    VANGUARD SERIES A PAT STD 37 3 PEG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 15, 2025

    POLISHED FINNED TIB TRAY 67MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 15, 2025

    VANGUARD CR POR FEM-RT 67.5

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 15, 2025