BEUDAMED
    10,000 results · 69ms · Sources: EU EUDAMED, US FDA

    Vereya ECO 80

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·NIPI-M AD·1 device

    Vereya Plus 80

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·NIPI-M AD·1 device

    Campímetro de Pantalla Tangente

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·General ASDE, S.A.·1 device

    Optotipo

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·General ASDE, S.A.·1 device

    Optotipo Retroiluminado

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·General ASDE, S.A.·1 device

    Deslumbrómetro

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·General ASDE, S.A.·1 device

    Vereya ECO

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·NIPI-M AD·1 device

    Vereya

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·NIPI-M AD·2 devices

    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

    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

    Catheter, Percutaneous (Valvuloplasty)

    FDA Pre-Market Approval
    FDA Class 3 ·INOUE-BALLOON Catheter

    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

    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(R) WITH CSTI(TM)

    Device, Dermal Replacement

    FDA Pre-Market Approval
    FDA Class 3 ·INTEGRA ARTIFICIAL SKIN DERMAL REGENERATION TEMPLATE