2,108 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Fluorescence In Situ Hybridization, Topoisomerase Ii Alpha, Gene Amplification And Deletion
FDA Pre-Market Approval
FDA Class 3
·DAKO TOP2A FISH PHARMDX KIT
Somatic Gene Mutation Detection System
FDA Pre-Market Approval
FDA Class 3
·THERASCREEN EGFR RGQ PCR KIT
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·SELECTSECURE & ANCHORING SLEEVE KIT
Fluorescence In Situ Hybridization, Chromosome 17p Deletion (Tp53)
FDA Pre-Market Approval
FDA Class 3
·Vysis CLL FISH Probe Kit
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·HORIZON(TM) YAG LASER MODEL 2000
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·HORIZON(TM) YAG LASER MODEL 2000
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·HORIZON(TM) YAG LASER MODEL 2000
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·HORIZON(TM) YAG LASER MODEL 2000
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·HORIZON(TM) YAG LASER MODEL 2000
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·HORIZON(TM) YAG LASER MODEL 2000
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·HORIZON(TM) YAG LASER MODEL 2000
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CapSure VDD 2 Lead, Service Kit-Pacemaker Repair Kit and Vitatron Brilliant S+ VDD Lead
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CapSure VDD-2 Lead, Service Kit-Pacemaker Repair Kit, and Vitatron Brilliant S+ VDD Lead
Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)
FDA Pre-Market Approval
FDA Class 3
·Alinity i HBsAg Qualitative II Reagent Kit and Alinity i HBsAg Qualitative II Confirmatory Kit
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CapSure VDD 2 Lead, Servuce Kit-Pacemaker Repair Kit, and Vitatron Brilliant S+ VDD Lead
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CapSure VDD-2 Lead, Service Kit-Pacemaker Repair Kit and Vitatron Brilliant S+ VDD Lead
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CapSure VDD-2 Lead, Service Kit-Pacemaker Repair Kit, and Vitatron Brilliant S+ VDD Lead
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CapSure VDD-2 Lead, Service Kit-Pacemaker Repair Kit, and Vitatron Brilliant S+ VDD Lead
Device, Thermal Ablation, Endometrial
FDA Pre-Market Approval
FDA Class 3
·AEGEA Vapor System, AEGEA Vapor Probe Procedure Kit, AEGEA Vapor Generator, AEGEA Vapor Generator Accessory Kit
Pump, Infusion, Implanted, Programmable
FDA Pre-Market Approval
FDA Class 3
·CODMAN 3000 SERIES CONSTANT-FLOW IMPLANTABLE INFUSION PUMP, MEDSTREAM REFILL KITS, SURESTREAM INTRASPINAL CATHETER KIT,C