BEUDAMED
    58 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    Filler, Bone Void, Synthetic Peptide

    FDA Pre-Market Approval
    FDA Class 3 ·PearlMatrix™ Bone Graft

    Filler, Bone Void, Synthetic Peptide

    FDA Pre-Market Approval
    FDA Class 3 ·PearlMatrix™ P-15 Peptide Enhanced Bone Graft (PearlMatrix™ Bone Graft)

    Filler, Bone Void, Synthetic Peptide

    FDA Pre-Market Approval
    FDA Class 3 ·PearlMatrix™ Peptide Enhanced Bone Graft

    ADULT ENDOTRACHEAL CLOSED SUCTION SYSTEM 24 HOURS, SIZE 14F

    FDA UDI
    Intersurgical Incorporated·05030267097807·ADULT ENDOTRACHEAL CLOSED SUCTION SYSTEM 24 HOU...

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517195159·MaXcess 4 Inserter, Locking Shim

    PLATE GUIDE

    FDA UDI
    Osteocentric Technologies, Inc.·00810189110298·PLATE GUIDE

    Histofluor® Primate Esophagus Autoantibody Fluorescent Test System

    FDA UDI
    IMMUNO CONCEPTS INC·M74912400011·Histofluor® Primate Esophagus Tissue BP FA Test...

    ARKEO, Wedge Fixation System

    FDA UDI
    Auxano Medical LLC·00810199190044·ARKEO Wedge Inserter Handle

    Forceps, Grasping, Down, 3mm, 28.5cm

    FDA UDI
    CLARUS MEDICAL, LLC·10810004820873·Forceps, Grasping, Down, 3mm, 28.5cm

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR32400011·SARA Distance ring 1 mm

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR32400010101·SARA Distance ring 1 mm

    Immunohistochemistry Test, Dna Mismatch Repair (Mmr) Protein Assay

    FDA Pre-Market Approval
    FDA Class 3 ·VENTANA MMR RxDx Panel

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·X STOP INTERSPINOUS PROCESS DECOMPRESSION SYSTEM

    X-STOP PEEK INTERSPINOUS SPACER

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NQO·February 1, 2019

    CARDIOSAVE HYBRID, 3.1 EDITION

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 23, 2024

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·X-STOP IPD SYSTEM

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·X-STOP INTERSPINOUS PROCESS DECOMPRESSION SYSTEM

    Immunohistochemistry Test, Dna Mismatch Repair (Mmr) Protein Assay

    FDA Pre-Market Approval
    FDA Class 3 ·VENTANA MMR RxDx Panel

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·X-STOP INTERSPINOUS PROCESS DECOMPRESSION SYSTEM

    Immunohistochemistry Test, Dna Mismatch Repair (Mmr) Protein Assay

    FDA Pre-Market Approval
    FDA Class 3 ·VENTANA MMR RxDx Panel Solid Tumors with dMMR status)