7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
COFIELD SHOULDER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690128779·Revision Fluted Offset Stem 18mm x 100mm x 4mm
CADD-VT, 5300 AMBULATORY INFUSION PUMP W/3050, 50M
FDA 510(k)
FDA Class 2
·General Hospital
PEPSODENT DENTURE CLEANSER PDP FORMULA
FDA 510(k)
FDA Class 1
·Dental
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 9, 2014
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
LAND AMERICA HEALTH & FITNESS·Product code FSA·December 3, 2012
OT VERIO2 METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 19, 2015