32 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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PRO.DUCT CATHETER, MODEL CTH03
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Custom Procedure Kit
FDA UDI
MEDIVATORS INC.·40677964001718·The ENDO CARRY-ON Procedure Kit contains all of...
Probe Tip 'Adult' PT-A 5pack
FDA UDI
PATH medical GmbH·04260223142888·
Golden Isles Pedicle Screw System
FDA UDI
Intelivation, LLC·G079C2520001350·Curved Ti Rod, 135mm
CURE LP
FDA UDI
MEDITECH SPINE, LLC·B167900001350·
QB1 NMES System
FDA UDI
Motive Health, Inc.·00854816006455·QB1 NMES System; 2X-LARGE, SHORT, RIGHT
PedFlex Flexible Nailing System
FDA UDI
ORTHOPEDIATRICS CORP.·00841132119457·ø3.5mm Flexible IM Nail Cap (2 Each)
OMNICARE DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (38 CM), MODEL 3555-38; MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (60 CM),
FDA 510(k)
FDA Class 2
·Neurology
FlowLogic Agile
FDA UDI
SONENDO, INC.·00810209420086·FlowLogic Agile Shaping File 15/.04, 25mm
CURE LP
FDA UDI
MEDITECH SPINE, LLC·B167S1900001350·
CURE LP
FDA UDI
SpineArt SA·07640270060590·ANTERIOR LUMBAR PLATE L35
PedFlex Flexible Nailing System
FDA UDI
ORTHOPEDIATRICS CORP.·00841132198179·Ø3.5 MM FLEXIBLE IM NAIL CAP (2 EACH)
QUADROX-ID ADULT DIFFUSION MEMBRANE OXYGENATOR
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY AG·Product code DTZ·June 25, 2015
NA
FDA UDI
Hangzhou AGS MedTech Co., Ltd.·06959664915905·
NA
FDA UDI
Hangzhou AGS MedTech Co., Ltd.·06959664915929·
QUADROX-ID DIFFUSION MEMBRANE OXYGENATOR
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY AG·Product code DTZ·June 25, 2015
ATS 3000 TOURNIQUET
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL·Product code KCY·February 14, 2013
LIGASURE ATLAS HANDSWITCHING 37CM
FDA Adverse Event
Malfunction
·COVIDIEN LLC (SHANGHAI)·Product code GEI·February 18, 2011
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code NIQ·February 19, 2008