BEUDAMED
    10,000 results · 55ms · Sources: EU EUDAMED, US FDA

    Acute Coronary Syndrome Event Detector

    FDA Pre-Market Approval
    FDA Class 3 ·AngelMed Guardian System

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VITALITY DS ICD SYSTEMS

    NEPHROCHECK Test Kit

    FDA UDI
    BIOMERIEUX SA·B0745000110·The Astute Medical NEPHROCHECK Test System is i...

    Prostrate Cancer Genes Nucleic Acid Amplification Test System

    FDA Pre-Market Approval
    FDA Class 3 ·PROGENSA PCA3 ASSAY

    Catheter, Coronary, Atherectomy

    FDA Pre-Market Approval
    FDA Class 3 ·ROTABLATOR ROTALINK PLUS ROTATIONAL ANGIOPLASTY SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK VISTA INTERBODY FUSION CAGE

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·ACTROS SLR+,KAIROS SL PULSE GENERATORS;SL 60-11,13,15 BP SINGLE PASS PACING LEAD;SWM 1000 B-G01.0.U

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·PRESTIGE LP(TM) CERVICAL DISC

    Programmer, Pacemaker

    FDA Pre-Market Approval
    FDA Class 3 ·VERITY ADX XL VDR MODEL 5456I PULSE GENERATOR

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·VERITY ADX XL VDR MODEL 5456I PULSE GENERATOR

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·DUAL INTERFIX-RP(TM) THREADED FUSION DEVICE

    Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·PRESTIGE LP CERVICAL DISC

    EARP INSTRUMENTS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00810135960649·RETRACTABLE OSTEOTOME. The EARP Interbody S...

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·SOLOX VDD PACING LEAD

    EARP INSTRUMENTS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00810135960571·EARP DISC SPACER 8MM The EARP Interbody Sys...

    EARP INSTRUMENTS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00810135960892·EARP, TRIAL 22X35X12 12° The EARP Interbody ...

    EARP INSTRUMENTS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00810135960618·EARP DISC SPACER INSERTER. The EARP Interbo...

    EARP INSTRUMENTS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00810135960854·EARP, TRIAL 18X35X14 12° The EARP Interbody ...

    EARP INSTRUMENTS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00810135960793·EARP, TRIAL 14X35X10 0° The EARP Interbody S...