BEUDAMED
    10,000 results · 145ms · Sources: EU EUDAMED, US FDA

    CAPCARD

    FDA 510(k)
    FDA Class 2 ·General Hospital

    COMPUTED TOMOGRAPHY ORIENTED ROTARY ARC

    FDA 510(k)
    FDA Class 2 ·Neurology

    CERTEX OCT SPINAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CLASSIC INTERMITTENT CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    FLEXICARE MEDICAL ENDOTRACHEAL TUBES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CO2 MONITORING LINE, CO2 MONITORING LINE WITH FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    O2 NASAL CANNULA WITH CO2 MONITORING

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DUALGUARD

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FLEXICARE BREATHING FILTERS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Flexicare Heated Wire Breathing Systems

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MosaiQ® AiPlex CTD

    Basic UDI-DI
    EU IVDR · Eu Ivd Class B ·AliveDx Suisse SA·1 device

    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