10 results
·
18ms
·
Sources: EU EUDAMED, US FDA
PowerWire® 14 Radiofrequency Guidewire Kit
FDA 510(k)
FDA Class 2
·Cardiovascular
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704282979·RETRACTOR MEYERDING SMALL 17 MILLIMETER X 55 M...
GIBSON HEALTHCARE
FDA UDI
BENCO DENTAL SUPPLY CO.·00366975012586·Gibson Healthcare Synthetic Granules, Synthetic...
ALP VasQcare Take Home System
FDA 510(k)
FDA Class 2
·Cardiovascular
ENCOR 7 GAUGE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
I-STAT CG8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·January 5, 2022
I-STAT EC8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·February 1, 2022
RESTORE RECHARGABLE NEUROSTIMULATOR
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 8, 2011
HEARTSTART FRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 5, 2014
UNICEL® DXC 800 SYNCHRON® SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code JGS·July 29, 2013