8 results
·
25ms
·
Sources: EU EUDAMED, US FDA
ACUTE CARDIAC CARE SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
CoRoent
FDA UDI
Nuvasive, Inc.·00887517821799·Interlock II Trial, 6x17x14mm 10° Stop
Symmetry Polokoff
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482125861·Symmetry® Rasp, Polokoff, Double-Ended, 5 mm an...
DAR-9400F
FDA 510(k)
FDA Class 2
·Radiology
Alivio Ventricular Catheter and Flusher System (Alivio System)
FDA 510(k)
FDA Class 2
·Neurology
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 25, 2014
QUATTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 2, 2012
ACCU-CHEK AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·September 18, 2007