824 results
·
41ms
·
Sources: EU EUDAMED, US FDA
CLARION II HI-RES COCHLEAR IMPLANT
FDA Adverse Event
Injury
·ADVANCED BIONICS·Product code MCM·July 30, 2005
HI (BTE)
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·SBO Hearing A/S·221 devices
HI (BTE)
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·SBO Hearing A/S·126 devices
HI (BTE)
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·SBO Hearing A/S·2050 devices
HI (BTE)
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·SBO Hearing A/S·1253 devices
HI (BTE)
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·SBO Hearing A/S·1525 devices
HI (BTE)
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·SBO Hearing A/S·610 devices
MED-EL COMBI 40+ CPCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·December 2, 2009
SONIC INNOVATIONS, INC.
FDA Adverse Event
Malfunction
·SONIC INNOVATIONS, INC.·Product code ESD·March 19, 2012
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·March 17, 2017
RESOUND
FDA Adverse Event
Injury
·GN HEARING A/S·Product code OSM·April 27, 2022
RESOUND
FDA Adverse Event
Injury
·GN HEARING A/S·Product code OSM·April 1, 2022
GN RESOUND
FDA Adverse Event
Injury
·GN HEARING A/S·Product code OSM·July 14, 2022
HILT FAMILY LASER: HILT I, HILT II, HILT III
FDA 510(k)
FDA Class 2
·Physical Medicine
IBT Scientific
FDA registration
IBT Scientific·5 products·🇺🇸 United States
HINT AUDIOMETER, OR HINT
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Power Dental USA
FDA UDI
Power Dental U.S.A. Inc.·D9439008BIBT00·PERIOSTEAL ELEVATORS SET (11 PCS)
Dream by 3D Dental
FDA UDI
3D DENTAL DESIGNS AND DEVELOPMENT, LLC·00817169028000·DREAM INTERDENTAL BRUSH TAPERED BOX/72 GREEN
HIP Cleaning Solution
FDA UDI
Dent4You AG·07640397422332·Hydrim Cleaning Solution with Instrument Protec...
'HILT-WAY' RESUSCITATOR
FDA 510(k)
FDA Class 1
·Anesthesiology