357 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·IS-1 Connector Port Pin Plug Kit, Sprint Quattro Lead
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·PIN PLUG, DF-1 Y-ADAPTER/ EXTENDER, LEAD ASSEMBLY SILICONE DEFIBRILLATOR
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·AcrySof IQ Aspheric IOL with the UltraSert Pre-loaded Delivery System
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF IQ TORIC IOL WITH THE ULTRASERT PRE-LOADED DELIVERY SYSTEM
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·ACE HEADER/TRANSVENE DEFIBRILLATION LEAD/LEAD END PIN CAP/UPSIZING SLEEVE
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
FDA Pre-Market Approval
FDA Class 3
·Accessory Kit Suture Sleeve Stabilizer and Accessory Terminal Pin Fixation Tool
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·LEAD END PIN, ACTIVE CAN EMULATOR HEADER, SIZING & UPSIZING SLEEVE
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·HOYA iSert 250/251 and Clarisert Pre-Loaded IOL Injector System
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·AcrySof IQ Aspheric IOL with the UltraSert Pre-Loaded Delivery System
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF IQ TORIC IOL WITH THE ULTRASERT PRE LOADED DELIVERY SYSTEM MODELS
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·ACCESSORY (UPSIZING SLEEVE) ACE/ACE 5434T/ACE HEADER/LEAD END PIN CAP
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Mi1260 SONATA 2 Cochlear Implant and Mi1250 SYNCHRONY 2 (PIN) Cochlear Implant
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·AcrySof® IQ Aspheric IOL with the UltraSert Pre-Loaded Delivery System
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