2,575 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·PROFILE(TM) MD (MODELS V-186F AND V-186HV3), PHOTON(TM) DR (MODEL V-230HV) AND PHOTON(TM) U VR/DR IMPLANTABLE CARDIOVER)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VENTAK PRIZM VR, PRIZM DR, PRIZM HE VR, PRIZM HE DR, PRIZM 2 VE, PRIZM 2 DR, PRIZM AT ICDS
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
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·PG ACCOLADE DR, PG ACCOLADE SR, PG ALTRUA 2 DR, PG ALTRUA 2 SR, PG ESSENTIO DR, PG ESSENTIO SR, PG PROPONENT DR, and PG
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·Acticor 7 DR-T DF4 ProMRI, Rivacor 3 DR-T DF4 ProMRI, Rivacor 5 DR-T DF4 ProMRI, Rivacor 7 DR-T DF4 ProMRI, Acticor 7 HF
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Enticos 4 DR, Enticos 4 D, Enticos 4 SR, Enticos 4 S, Edora 8 DR-T, Evity 8 DR-T, Enitra 8 DR-T, Enticos 8 DR-T, Evity 6
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·OVATIO DR MODEL 6550 AND OVATIO VR MODEL 6250 ICDS, ELAVIEW 1.32 UG2 PROGRAMMING SOFTWARE AND CPR3 PROGRAMMING HEAD
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Edora 8 DR-T, Evity 8 DR-T, Enitra 8 DR-T, Evity 6 DR-T, Enitra 6 DR-T, Edora 8 DR, Enitra 6 DR, Enticos 4 DR, Enticos 4
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Edora 8 DR-T, Evity 8 DR-T, Enitra 8 DR-T, Evity 6 DR-T, Enitra 6 DR-T, Edora 8 DR, Enitra 6 DR, Enticos 4 DR, Enticos 4
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·HYALGAN
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·HYALGAN
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·HYALGAN(R)
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·HYALGAN®
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·HYALGAN