BEUDAMED
    39 results · 28ms · Sources: EU EUDAMED, US FDA

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    Agent, Absorbable Hemostatic, Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·SUPERSTAT

    Agent, Absorbable Hemostatic, Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·SUPERSTAT

    Agent, Absorbable Hemostatic, Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·SUPERSTAT

    Agent, Absorbable Hemostatic, Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·SUPERSTAT

    Agent, Absorbable Hemostatic, Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·SUPERSTAT

    Agent, Absorbable Hemostatic, Collagen Based

    FDA Pre-Market Approval
    FDA Class 3 ·SUPERSTAT

    Hader

    FDA UDI
    STERNGOLD DENTAL LLC·00841549115875·Hader Vertical Starter Kit

    APEX Spine System

    FDA UDI
    SPINECRAFT, LLC·00193082014789·APEX Ti Poly Screw Dia.10.0, 40mm

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540730794·PEEK CUSTOMIZED CRANIAL IMPLANT KIT, XL

    APEX Spine System

    FDA UDI
    SPINECRAFT, LLC·M824P6100401·Polyaxial Pedicle Screw, 10.0mm x 40mm

    Esthetic Abutment H3mm Burn-Out

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011130·

    Esthetic Abutment H3mm Burn-Out

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118141617·Esthetic Abutment H3mm Burn-Out

    APEX Spine System

    FDA UDI
    SPINECRAFT, LLC·M824SCP6100401·Polyaxial Pedicle Screw, 10.0 x 40mm

    Electroplated diamond RA 810 040

    FDA UDI
    Diaswiss SA·07630049992689·Dental diamond instrument for intraoral use

    Momentum

    FDA UDI
    Ulrich Medical Usa, Inc.·00814386025829·Navigated tap, Ø 4.0mm, non-cannulated, 1/4"-sq...

    ACRIDINE ORANGE STAIN

    FDA 510(k)
    FDA Class 1 ·Hematology

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC VASCULAR COMPLETE SE VASCULAR STENT SYSTEM

    Sharps Needle Destruction Device

    FDA Pre-Market Approval
    FDA Class 2 ·THE DISINTEGRATOR INSULIN NEEDLE DESTRUCTION DEVICE

    ACS RX LIFESTREAM CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·ACS/DVI·Product code LOX·March 14, 1997

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·COMPLETE SE VASCULAR STENT SYSTEM-SFA AND PPA