1,398 results
·
46ms
·
Sources: EU EUDAMED, US FDA
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·Aptima HCV Quant Dx Assay
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·Aptima HCV Quant Dx Assay
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·Aptima HCV Quant Dx Assay
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·Aptima HCV Quant Dx Assay
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·Aptima HCV Quant Dx Assay
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·Aptima HCV Quant DX Assay
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
FDA Pre-Market Approval
FDA Class 3
·Tendril DX Endocardial Pacing Leads
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·Aptima HCV Quant Dx Assay
HDX WILL Europe GmbH
Importer
🇩🇪 Germany·1 Manufacturer
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·llesto 7 VT-T / 5 VR-T , 7 VR-T DX; Ifora 7 VR-T /5 VR-T /7 VR-T DX , 5 VR-T DX ; Itrevia 7 VT-T/ DX (GBLi), Intica 5 VR
VERTEXA® Anorexie et Boulimie
Basic UDI-DI
EU MDR
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Eu Md Class 1
·VERTEXA·1 device
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·INTELLANAV STABLEPOINT Ablation Catheter & Force Sensing System on the RHYTHMIA HDX Mapping System
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·LUMAX 540 VR-T DX ICD
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·PASSIVE PLUS DX FAMILY OF LEADS
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·TENDRIL/PASSIVE PLUS/AV PLUS DX
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·TENDRIL/PASSIVE PLUS/AV PLUS DX
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·TENDRILL PASSIVE PLUS/AU PLUS DX
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·TENDRILL PASSIVE PLUS/AU PLUS DX
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·PASSIVE PLUS DX FAMILY OF LEADS
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·AV PLUS DX MODEL 1368 LEAD