10 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ulricheasyINJECT Max 2M (XD 10140); ulricheasyINJECT Max 3 (XD 10150); ulricheasyINJECT Max 3 (XD 10180)
FDA 510(k)
FDA Class 2
·Cardiovascular
ceraMotion®
FDA UDI
DENTAURUM GmbH & Co.KG·J011252281200·ceraMotion® Me Incisal Value 2, 20 g / dental c...
Pyrenees Cervical Plate System
FDA 510(k)
FDA Class 2
·Orthopedic
EMBRACE WETBOND CLEAR SEALANT
FDA 510(k)
FDA Class 2
·Dental
OCTRODE LEAD KIT, 60CM LENGTH
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LGW·May 7, 2024
BD MICRO-FINE¿ INSULIN PEN NEEDLE
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FMI·February 8, 2018
DAVINCI XI
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·June 9, 2025
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·November 14, 2014
NC TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·September 17, 2011
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 29, 2013