40 results
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20ms
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Sources: EU EUDAMED, US FDA
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FDA Pre Market Approval
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Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·KELVIN MODEL 500 UNIPOLAR CARDIAC PULSE GENERATOR
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·KELVIN MODEL 500 UNIPOLAR CARDIAC PULSE GENERATOR
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·KELVIN (R) PACING SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MODEL K (UNIPOLAR) & M (BIPOLAR) ENDOCARDIAL LEADS
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·KELVIN MODEL 500 UNIPOLAR CARDIAC PULSE GENERATOR
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·KELVIN MODEL 500 UNIPOLAR CARDIAC PULSE GENERATOR
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MODEL Q (UNIPOLAR) & R (BIPOLAR) ENDOCARDIAL LEADS
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·KELVIN MODEL 500 UNIPOLAR CARDIAC PULSE GENERATOR
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·KELVIN(R) MODEL 513 UNIPOLAR AND MODEL 514 BIPOLAR CARDIAC PULSE GENERATORS.
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·KELVIN MODEL 500 UNIPOLAR CARDIAC PULSE GENERATOR
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·KELVIN MODEL 500 UNIPOLAR CARDIAC PULSE GENERATOR
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·NEODYMIUM: YAG OPHTHALMIC LASER SYSTEM 9900
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·NEODYMIUM: YAG OPHTHALMIC LASER SYSTEM 9900
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·NEODYMIUM: YAG OPHTHALMIC LASER SYSTEM 9900
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·NEODYMIUM: YAG OPHTHALMIC LASER SYSTEM 9900
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SILCON(R) (SILAFILCON A) CONTACT LENS DAILY WEAR
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·NEODYMIUM: YAG OPHTHALMIC LASER SYSTEM 9900
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·NEODYMIUM: YAG OPHTHALMIC LASER SYSTEM 9900
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·NEODYMIUM: YAG OPHTHALMIC LASER SYSTEM 9900
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·NEODYMIUM: YAG OPHTHALMIC LASER SYSTEM 9900