14 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CATH LAB MONITORING CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Ormco
FDA UDI
ORMCO CORPORATION·00889989074451·FORESTADENT SMALL CLEAT
ENI BLOOD UREA NITROGEN REAGENT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
A3B
FDA 510(k)
FDA Class 1
·Microbiology
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082841·Screw, pre-fixation, Ø 6.5 mm, length 55 mm, no...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082834·Screw, pre-fixation, Ø 6.5 mm, length 50 mm, no...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082858·Screw, pre-fixation, Ø 6.5 mm, length 60 mm, no...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082803·Screw, pre-fixation, Ø 6.5 mm, length 35 mm, no...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082810·Screw, pre-fixation, Ø 6.5 mm, length 40 mm, no...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082797·Screw, pre-fixation, Ø 6.5 mm, length 30 mm, no...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082827·Screw, pre-fixation, Ø 6.5 mm, length 45 mm, no...
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·June 19, 2014
FREESTYLE NAVIGATOR
FDA Adverse Event
Injury
·Product code MDS·December 21, 2012
6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code MGB·October 20, 2010