BEUDAMED
    45 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.

    NVISION VLE IMAGING SYSTEM, NVISION VLE CATHETER

    FDA 510(k)
    FDA Class 2 ·Radiology

    PerFix

    FDA UDI
    Davol Inc.·00801741016615·PerFix Plug, 1.6" x 1.9" (4.1 cm x 4.8 cm), Lar...

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317361714·

    PERFIX PLUG

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·May 7, 2018

    INFINITY MICRO2+

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FLEXTIME FAST & SCAN PUTTY, FLEXTIME FAST & SCAN LIGHT FLOW, FLEXTIME FAST & SCAN MEDIUM FLOW

    FDA 510(k)
    FDA Class 2 ·Dental

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 9, 2025

    0112770-BARD MESH LARGE PREFIX

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (PUERTO RICO)·Product code FTL·October 30, 2000

    0112770-BARD MESH LARGE PREFIX

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (PUERTO RICO)·Product code FTL·June 18, 2003

    0112770-BARD MESH LARGE PREFIX

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (PUERTO RICO)·Product code FTL·June 18, 2003

    0112770-BARD MESH LARGE PREFIX

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (PUERTO RICO)·Product code FTL·June 11, 2003

    0112770-BARD MESH LARGE PREFIX

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (PUERTO RICO)·Product code FTL·June 11, 2003

    0112770-BARD MESH LARGE PREFIX

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (PUERTO RICO)·Product code FTL·April 6, 2001

    0112770-BARD MESH LARGE PREFIX

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (PUERTO RICO)·Product code FTL·April 10, 2001

    PARIETEX

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·November 12, 2021

    BARD MESH PERFIX PLUG

    FDA Adverse Event
    BARD DAVOL, INC.·Product code FTL·January 30, 2018

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code INM·May 14, 2013

    GLOBAL AP HUMERAL STEM 12MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWS·May 18, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 15, 2008

    PERFIX PLUG

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·November 26, 2019