549 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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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 FIBER PLASMAFILTER
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 DERMAL REGENERATION TEMPLATE
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 TPE 2000 Set
Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA Pre-Market Approval
FDA Class 3
·NEW JERSEY LCS(R) UNICOMPARTMENTAL KNEE
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·PRISMAFLEX TPE 2000 Set
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 Prismaflex TPE 2000 Set
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
·Prismaflex TPE2000 Set
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
·PLASMAFLO OP-05W (A)
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE
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 ARTIFICIAL SKIN DERMAL REGENERATION TEMPLATE
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·PROSORBA COLUMN