440 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Stimulator, Electrical, Implanted, For Parkinsonian Tremor
FDA Pre-Market Approval
FDA Class 3
·Legacy MDT Pocket Adapter
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·HYDROXYPROPYLMETHYLCELLULOSE 20MG/ML, MDR CORP.
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·EMBLEM S-ICD, EMBLEM MRI S-ICD,
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·COLLAMER UV-ABSORBING POSTERIOR CHAMBER IOL
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SILICON UV-ABSORBING POSTERIOR CHAMBER IOL
Sealant, Polymerizing
FDA Pre-Market Approval
FDA Class 3
·COSEAL SURGICAL SEALANT & ACCESSORIES
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·SPRINT QUATTRO LEAD, SPLITTER/ADAPTOR, DF-4 IMPLANT TOOL KIT FOR MDT LEADS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·EASYTRAK 3 IS-1 LEADS
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·ACUITY STEERABLE IS-1 LEADS
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC(R) MDL 6966, 6936, 6963 TRANSVENE(R) AND MODEL 6939 AND 6999 SUBCUTANEOUS PATCH LEADS.
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CADET V-105 C AND D AND V-115 C AND D PULSE GENERATORS & SOFTWARE VERSION 4.1 FOR THE PROGRAMMER MDL PR-1500
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·PLASMAFLO
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE, INTEGRA MESHED DERMAL REGENERATION TEMPLATE
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE - TERMINALLY STERILIZED (IDRT-TS)
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA DERMAL REGENERATION TEMPLATE
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·GAMBRO PLASMAFILTER, PF2000N
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA ARTIFICIAL SKIN DERMAL REGENERATION TEMPLATE
Device, Dermal Replacement
FDA Pre-Market Approval
FDA Class 3
·INTEGRA(R) DERMAL REGENERATION TEMPLATE,INTEGRA(R) MESHED DERMAL REGENERATION TEMPLATE,OMNIGRAFT (TM) DERMAL REGENERATIO
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·GAMBRO PRISMAFLEX TPE 2000 SET
Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma
FDA Pre-Market Approval
FDA Class 3
·PRISMAFLEX TPE2000 SET