3,190 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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RETROX RX 53-BP, RETROX RX 60-BP, RETROX RX 45-JBP, RETROX RX 53-JBP MODEL NUMBERS 124 396, 124 397, 124 395, 124 000
FDA 510(k)
FDA Class 3
·Cardiovascular
MINIFLEX MODEL 340, 341, AND 342 PULSE GENERATORS
FDA 510(k)
FDA Class 3
·Cardiovascular
OPUS S MODEL 4121 AND 4124 PACEMAKERS
FDA 510(k)
FDA Class 3
·Cardiovascular
DF-1 TERMINAL CAP
FDA 510(k)
FDA Class 3
·Cardiovascular
JUMP START, MODEL 970300
FDA 510(k)
FDA Class 3
·Cardiovascular
HEWLETT-PACKARD M2475B WITH 12-LEAD OPTION (#C90) CODEMASTER 100 CONITOR/DEFIBRILLATOR
FDA 510(k)
FDA Class 3
·Cardiovascular
FIRSTSAVE BIPHASIC MODELS 9200 AND 9210
FDA 510(k)
FDA Class 3
·Cardiovascular
Pump, Infusion, Implanted, Programmable
FDA Pre-Market Approval
FDA Class 3
·MEDSTREAM PROGRAMMABLE INFUSION SYSTEM
System, Hemodynamic, Implantable
FDA Pre-Market Approval
FDA Class 3
·CARDIOMEMS
Implanted Brain Stimulator For Epilepsy
FDA Pre-Market Approval
FDA Class 3
·NEUROPACE RNS SYSTEM
Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled
FDA Pre-Market Approval
FDA Class 3
·MEMORYGEL BREAST IMPLANT
Barrier, Absorbable, Adhesion
FDA Pre-Market Approval
FDA Class 3
·INTERCEED (TC7) ABSORBABLE ADHESION BARRIER
Lens, Contact (Rigid Gas Permeable), Extended Wear
FDA Pre-Market Approval
FDA Class 3
·FluoroPerm30 (paflufocon C), FluoroPerm60 (paflufocon B), FluoroPerm92 (paflufocon A), Paragon HDS (paflufocon B) Rigid
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·DUETT PRO SEALING DEVICE MODEL 1010
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·XIENCE PRIME AND XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM (EECSS)
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·DRIVER AND MICRO-DRIVER CORONARY STENT SYSTEMS
System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection
FDA Pre-Market Approval
FDA Class 3
·COLOGUARD
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC AT500 DDDRP PACING SYSTEM
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC ACTIVA TREMOR CONTROL SYSTEM
Filler, Bone Void, Synthetic Peptide
FDA Pre-Market Approval
FDA Class 3
·i-FACTOR Peptide Enhanced Bone Graft