4,936 results
·
43ms
·
Sources: EU EUDAMED, US FDA
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·Attain Ability Lead
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·Attain Ability Lead and Attain Performa Lead
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·ACUITY STEERABLE
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC ATTAIN STARFIX MODEL 4195 LEADS
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·Attain Ability Lead and Attain Performa Lead
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·INSYNC CRT-P & INSYNC III CRT-P
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·CONSULTA CRT-P, SYNCRA CRT-P
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·ATTAIN ABILITY MODEL 4X96 LEAD
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·CONSULTA CRT-P, SYNCRA CRT-P
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·ATTAIN ABILITY LEADS
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·INSYNC/INSYNC III/CONSULTA/SYNERA CRT-PS
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·Attain Ability Lead
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·ATTAIN STARFIX MODEL 4195 LEAD
Standard anti-Tg IgG - Standard anti-Tg IgG
Basic UDI-DI
EU IVDR
·
Eu Ivd Class A
·ABD SRL·1 device
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·P880086 Endurity PM1162, PM2162; Endurity Core PM1140, PM2140; AV Plus Dx Lead 1368; Verity ADx XL 5357M/S, 5356, 5256,
Phantom
FDA UDI
medimaps group SA·B214OSPTM3·
DJO EMPOWR REVISION KNEE, POST AUG TRIALS, SZ 2/3, 10MM,LL (800-05-108)
FDA registration
Straits Orthopaedics (MFG) Sdn Bhd·1 product·🇲🇾 Malaysia
DJO EMPOWR REVISION KNEE, POST AUG TRIALS, SZ 2/3, 10MM,LL (800-05-108)
FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia
Somatic Gene Mutation Detection System
FDA Pre-Market Approval
FDA Class 3
·CRCDx RAS Mutation Detection Assay Kit
Plasminogen, Antigen, Antiserum, Control
FDA classification
FDA Class 1
·Plasminogen, Antigen, Antiserum, Control