3,100 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·PROVISC OPHTHALMIC VISCOSURGICAL DEVICE
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·Healon Ultimate Dual Pack, HEALON, HEALON GV, HEALON5, and Healon Duet Dual Pack products
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·REVO MRI
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·VISCOAT OPHTHALMIC VISCOSURGICAL DEVICE
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·COGNIS CRT MODELS N118, N19
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·REVO MRI SURESCAN IPG
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VERSATRAX MODEL 7000 UNIVERSAL A-V PULSE GENERATOR
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AFP PACING SYSTEM
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·EFH-16; S 60-K; S 60-J; S 60-S
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·COSMOS II MODELS 284-05,283-03 PULSE GENERATOR
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·ESSENTIO MRI, PROPONENT MRI, and ACCOLADE MRI Pacemakers
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·HYVISC(R)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·REFLEX MODEL 8223E
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Ingevity MRI Leads and Slit Suture Sleeve Accessory for Ingevity Leads
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VITALITY HE, RENEWAL 3 AND RENEWAL 3RF FAMILIES OF ICDS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VENTAK AV AICD SYSTEM
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VIGOR MODEL 2880 SOFTWARE APPLICATION (REV 3.0)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AUTIMA(TM) MODEL 2251 & MODEL 2600
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·HYDROXYPROPYLMETHYLCELLULOSE 2% OCCUCOAT (R)
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·OCUCOAT OPHTHALMIC VISCOSURGICAL DEVICE