549 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL (TM)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL VHD
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL (VASCULAR HEMOSTASIS DEVICE)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL (TM)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL 4-5 FRENCH SYSTEM
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CADET V-105 C AND D AND V-115 C AND D PULSE GENERATORS & SOFTWARE VERSION 4.1 FOR THE PROGRAMMER MDL PR-1500
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·PLASMAFLO
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·NATURAL-KNEE(R) WITH CSTI(TM)
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE, INTEGRA MESHED DERMAL REGENERATION TEMPLATE
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE - TERMINALLY STERILIZED (IDRT-TS)
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·GAMBRO PLASMAFILTER, PF2000N
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA ARTIFICIAL SKIN DERMAL REGENERATION TEMPLATE
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA(R) DERMAL REGENERATION TEMPLATE,INTEGRA(R) MESHED DERMAL REGENERATION TEMPLATE,OMNIGRAFT (TM) DERMAL REGENERATIO
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·GAMBRO PRISMAFLEX TPE 2000 SET
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·PRISMAFLEX TPE2000 SET
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·Gambro Prismaflex TPE2000 Set
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA ARTIFICIAL SKIN DERMAL REGENERATION TEMPLATE
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·NATURAL-KNEE AND NATURAL-KNEE II