BEUDAMED
    15 results · 34ms · 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.

    TELEMEDIC TELERADIOLOGY SYSTEM

    FDA 510(k)
    FDA Class 1 ·Radiology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471121942·K-WIRE - DOUBLE TROCAR 1.1mm DIA x 125mm

    NERVUS MONITOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    EDWARDS PERCUTANEOUS SHEATH INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AGC DA2000 KN TIB BRG 71/75X14

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·August 31, 2016

    BIOMET AGC V2 INTERLOK TIBIAL 22X 67MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HRY·June 16, 2017

    E1 RINGLOC BIPOLAR 28X51MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LZO·June 17, 2019

    AGC V2 INTERLOK TIB 10X 71MM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code HRX·May 19, 2017

    4.5MM LCP® CURVED CONDYLAR PLATE 10 HOLES/242MM-RIGHT

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code KTT·January 17, 2013

    MINI-CAP, DISCONNECT W/PVP-1SOLUTION

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·December 13, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 9, 2014

    AGC V2 INTERLOK TIB 8 X 75MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·April 12, 2017

    BIOMEX SHELL PC DIA48MM LN 22

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 2, 2015

    AGC V2 INTERLOK TIB 8 X 79MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·March 22, 2016

    AGC REVISION KNEE TIBIAL AUGMENTATION

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code JWH·June 28, 2017