11 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Avanos* CORTRAK* 2 Enteral Access System (EAS)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Bernafon
FDA UDI
Sbo Hearing A/S·05714464011254·EASYCONTROL-A 2.3.0 ANDROID
ELMED
FDA UDI
ELMED INCORPORATED·00842180124509·5 MM DIA., 33 CM, INSULATED CONE ELECTRODE, RE...
VEO® Lateral Interbody Fusion System
FDA UDI
Choice Spine, LP·00840996134613·LATERAL, COBB ELEVATOR, REV.SLAP, 16MM
BNA Platform
FDA 510(k)
FDA Class 2
·Neurology
X-IMAGE DIGITAL X-RAY SYSTEM
FDA 510(k)
FDA Class 2
·Dental
SCREWDRIVER, SELF-HOLDING, EXTRA SHORT SCREWDRIVER, SELF-HOLDING 3.5 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·November 3, 2014
IVT DISPOSABLE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code LHI·August 23, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013
BD CATHENA¿ SAFETY IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·July 7, 2022
BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Co.·April 21, 2021