505 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Scaffold, Dissection Repair
FDA Pre-Market Approval
FDA Class 3
·Tack Endovascular System (4F, 1.5-4.5mm)
Scaffold, Dissection Repair
FDA Pre-Market Approval
FDA Class 3
·Tack Endovascular System (6F)
Scaffold, Dissection Repair
FDA Pre-Market Approval
FDA Class 3
·Tack Endovascular System (6F)
Scaffold, Dissection Repair
FDA Pre-Market Approval
FDA Class 3
·Tack Endovascular System (6F)
Scaffold, Dissection Repair
FDA Pre-Market Approval
FDA Class 3
·Tack Endovascular System (6F)
Instrument, Glucose, Noninvasive Technology
FDA Pre-Market Approval
FDA Class 3
·GLUCOWATCH AUTOMATIC GLUCOSE BIOGRAPHER
Scaffold, Dissection Repair
FDA Pre-Market Approval
FDA Class 3
·Tack Endovascular System (6F)
Scaffold, Dissection Repair
FDA Pre-Market Approval
FDA Class 3
·Tack Endovascular System (4F, 1.5-4.5mm)
Scaffold, Dissection Repair
FDA Pre-Market Approval
FDA Class 3
·Tack Endovascular System (4F, 1.5-4.5mm)
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSUREFIX LEAD; CAPSUREFIX NOVUS LEAD; SUREFIX LEAD;VITATRON CRYSTALLINE ACTIVE FIXATION LEAD; VITATRON CRYSTALLINE ACT
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSUREFIX LEAD, CAPSUREFIX NOVUS LEAD,SUREFIX LEAD, VITATRON CRYSTALLINE ACTIVE FIXATION LEAD, VITATRON CRYSTALLINE ACT
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·ISOLINE 2CR DEFIBRILLATION LEADS MODELS 2CR5, 2CR6 AND 2CR7
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·ISOLINE 2CR DEFIBRILLATION LEADS
Implant, Intragastric For Morbid Obesity
FDA Pre-Market Approval
FDA Class 3
·Lap-Band Adjustable Gastric Banding System
System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection
FDA Pre-Market Approval
FDA Class 3
·COLOGUARD
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·VITRAX SODIUM HYALURONATE
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·MODEL AC-21 OMNIFIT ANTERIOR CHAMBER
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·MODEL 304 (ULTRA C-LOOP)
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·CM(TM) LENSES
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·MODEL 304 (ULTRA C-LOOP)