1,516 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·SCS NEUROSTIMULATORS IMPLANTABLE RESTORE FAMILY
Sensor, Glucose, Invasive
FDA Pre-Market Approval
FDA Class 3
·Medtronic MiniMed iPro2 CGM System with Enlite Sensor
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·ACUVUE(R) (ETAFILCON A) EXTENDED WEAR CONTACT LENS (CLEAR AND TINTED WITH UV BLOCKER)
Automated Insulin Dosing , Threshold Suspend
FDA Pre-Market Approval
FDA Class 3
·Medtronic MiniMed 630G System
Sensor, Glucose, Invasive
FDA Pre-Market Approval
FDA Class 3
·Medtronic MiniMed Paradigm Real-Time Revel System
Automated Insulin Dosing , Threshold Suspend
FDA Pre-Market Approval
FDA Class 3
·Medtronic MiniMed 530G System
Implant, Anti-Gastroesophageal Reflux
FDA Pre-Market Approval
FDA Class 3
·LINX REFLUX MANAGEMENT SYSTEM
Automated Insulin Dosing Device System, Single Hormonal Control
FDA Pre-Market Approval
FDA Class 3
·Medtronic MiniMed 670G System
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
FDA Pre-Market Approval
FDA Class 3
·STELID II/STELIX/STELIX II ENDOCARDIAL PACING LEAD
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·FOCUS NIGHT & DAY (LOTRAFILCON A) EXTENDED WEAR SOFT CONTACT LENSES
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·FOCUS NIGHT AND DAY (LOTRAFILCON A AND B) EXTENDED WEAR SOFT CONTACT LENSES
Ventricular (Assist) Bypass
FDA Pre-Market Approval
FDA Class 3
·EXCOR® Pediatric Ventricular Assist Device
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·Orsiro Sirolimus Eluting Coronary Stent System
Stimulator, Autonomic Nerve, Implanted For Epilepsy
FDA Pre-Market Approval
FDA Class 3
·VNS THERAPY SYSTEM
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·SCS Implantable Neurostimulators
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·ACTROS SLR+,KAIROS SL PULSE GENERATORS;SL 60-11,13,15 BP SINGLE PASS PACING LEAD;SWM 1000 B-G01.0.U
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·HeartSine Technologies LLC's samaritan Public Access Automated External Defibrillators (SAM 350P, SAM 360P and SAM 450P)
HEARTSINE SAMARITAN PAD 350P
FDA 510(k)
FDA Class 3
·Cardiovascular
Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
FDA Pre-Market Approval
FDA Class 3
·VARIOUS FAMILIES OF CRT-ICD'S
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VITALITY AVT AND THE PROGRAMMER SOFTWARE APPLICATION MODEL 2812