40 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TQ HBA1C GEN3
FDA 510(k)
FDA Class 2
·Hematology
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169373341·BLADE 5102914 29MM WIDE VESSELBLADE 14CM
CRYOPEN CRYOSURGICAL SYSTEM, K102214
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LEONE SPA
FDA UDI
LEONE SPA·08033707094937·IMPLANT 2.9 W/CAPS D2,9 L14MM
LEONE SPA
FDA UDI
LEONE SPA·08033707094555·IMPLANT 2.9 W/CAP D2,9 L14MM
Monster® Screw System
FDA UDI
Paragon 28, Inc.·00889795040633·Drill, 2.9 x 140mm, Cannulated, 3/16" Sq. Conne...
Paragon 28
FDA UDI
Provision·B504OMP9911029140·
Plateau Spacer System
FDA UDI
Life Spine, Inc.·00190837026912·PLATEAU Interbody, Curved, Bulleted, 11mm 29mm ...
TENS STIMULATOR, MODELS 2800 AND 3000
FDA 510(k)
FDA Class 2
·Neurology
SONICWAVE SONIC PLAQUE REMOVER
FDA 510(k)
FDA Class 1
·Dental
HLM TUBING SET
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 1, 2015
VKMO 70000 #QUADROX-I HMO 70000+VHK71
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTN·February 23, 2015
BO-HQV 70600#ADULT PACK
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTN·February 19, 2015
BO-HQV #70600ADULT PACK
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY AG·Product code DTN·March 4, 2015
BO-HQV 70600#ADULT PACK
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DWE·March 27, 2015
BO-HQV 70600#ADULT PACK
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DWE·April 9, 2015
VKMO 11000
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 24, 2015
BO-HQV 70600 ADULT PACK
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTN·July 15, 2015
RESERVOIR VHK
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTN·July 28, 2015
VENOUS HARDSHELL CARDIOTOMY RESERVOIR
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTM·September 13, 2016