7,515 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
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 (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)
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·ISOLINE 2CR DEFIBRILLATION LEADS
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT STRIP BONE GRAFT MATRIX
Aortic Stent
FDA Pre-Market Approval
FDA Class 3
·Minima Stent System
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT SUBSTITUTE
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT MATRIX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT MATRIX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT STRIP BONE GRAFT MATRIX
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT(TM) BONE GRAFT SUBSTITUTE
Filler, Bone Void, Non-Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·COLLAGRAFT STRIP BONE GRAFT MATRIX
Aortic Stent
FDA Pre-Market Approval
FDA Class 3
·Minima Stent System