BEUDAMED
    11 results · 18ms · 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.

    HEMATOXYLIN

    FDA 510(k)
    FDA Class 1 ·Hematology

    ERA® Implant Abutment Standard 0°, 2mm Cuff (B)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549102370·Implant retained overdentures are an establishe...

    GoBack Crossing Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SV BRAIN ARRAY, SIEMENS 3T

    FDA 510(k)
    FDA Class 2 ·Radiology

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·December 23, 2025

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·November 21, 2025

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·April 30, 2025

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·March 6, 2025

    RECOVERCARE

    FDA Adverse Event
    Malfunction ·RECOVERCARE·Product code FNL·May 9, 2014

    MAXIMO II CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·October 31, 2012

    UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·August 23, 2010