BEUDAMED
    20 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 ×

    SKR 4000

    FDA 510(k)
    FDA Class 2 ·Radiology

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074465289·CDH HA COATED MAS 6.5X45

    Axcess Percutaneous Introducer

    FDA UDI
    ARGON MEDICAL DEVICES, INC.·00886333206902·Axcess Percutaneous Introducer with Multi-Purpo...

    NON-CHLORINATED, POLYMER COATED POWDER FREE NATURAL RUBBER LATEX EXAMINATION GLOVES AND PROTEIN LABELING CLAIM OF

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GOLD ANCHOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    FEMORAL POSTERIOR AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    TUBE, GASTROINTESTINAL (AND ACCESS)

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code KNT·November 21, 2008

    STEM EXTENSION STRAIGHT SPLINED UNCEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    FEMORAL DISTAL AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    FEMORAL DISTAL AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    SEE H10 NARRATIVE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    SEE H10 NARRATIVE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    TIBIA FIXED CEMENTED LEFT SIZE D STEM EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    TUBE, GASTROINTESTINAL (AND ACCESS)

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code KNT·October 24, 2008

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 22, 2014

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·August 4, 2011

    TOTAL ASR ACET IMP SIZE 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.·Product code KWA·June 26, 2013