9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
REPLACE TITANIUM IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
Reusable Instruments used with SOVEREIGN® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994320636·TRIAL 7964220 S 32X23 20MM 12 DEG
Bioseal Inc.
FDA UDI
BIOSEAL·00630094196428·Silastic Tubing 42"
PIONEER PRO-PUMP
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
SYNCHRON CX4-CE
FDA 510(k)
FDA Class 1
·Clinical Chemistry
AT HOME DRUG TEST PHARATECH
FDA Adverse Event
PHAMATECH·Product code MVO·September 24, 2003
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·February 15, 2013
LIFEPAK 15 MONITOR/DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·December 22, 2010
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 29, 2014