8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Mfinity Femoral System
FDA 510(k)
FDA Class 2
·Orthopedic
Instru-Safe Instrument Protection System
FDA 510(k)
FDA Class 2
·General Hospital
POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH PLASTICIZER EBN&BET
FDA 510(k)
FDA Class 1
·General Hospital
ONE TOUCH BASIC ENHANCED
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·June 6, 2003
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 5, 2014
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·September 8, 2011
HEARTSTART ONSITE
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 5, 2014
AMPLATZ
FDA Adverse Event
Malfunction
·COOK MEDICAL INCORPORATED·Product code DQX·July 19, 2013