7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Arm Blood Pressure Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
SILK ROAD ACCESS CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
DRI COTININE EIA ASSAY
FDA 510(k)
FDA Class 1
·Clinical Toxicology
MICROSENSOR VENTRICULAR CATHETER KIT
FDA Adverse Event
Malfunction
·CODMAN & SHURTLEFF, INC.·Product code GWM·November 6, 2008
TALENT THORACIC STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·August 12, 2011
TOTAL ASR FEM IMP SIZE 51
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KXA·July 16, 2013
CODMAN Disposable Perforator 11mm. Cranial Perforator.
FDA Enforcement
Class I
·Ongoing·Integra LifeSciences Corp. (NeuroSciences)·November 12, 2025