541 results
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17ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Pulse Generator, Permanent Implantable
Implant, Intragastric For Morbid Obesity
FDA Pre-Market Approval
FDA Class 3
·ORBERA Intragastric Balloon (IGB) System
Implant, Intragastric For Morbid Obesity
FDA Pre-Market Approval
FDA Class 3
·ORBERA® Intragastric Balloon (IGB) System
Implant, Intragastric For Morbid Obesity
FDA Pre-Market Approval
FDA Class 3
·Orbera® Intragastric Balloon (IGB) System
Implant, Intragastric For Morbid Obesity
FDA Pre-Market Approval
FDA Class 3
·ORBERA ® Intragastric Balloon (IGB) System
Implant, Intragastric For Morbid Obesity
FDA Pre-Market Approval
FDA Class 3
·ORBERA Intragastric Balloon (IGB) System, Endoline Punc
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·(LGW, QRB) - Master Restore Spinal Cord Stimulation Systems
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·Ilivia Neo 7 HF -T QP, Ilivia Neo 7 HF -T, Intica Neo 7 HF -T QP, Intica Neo 7 HF -T, Intica Neo 5 HF -T QP, Intica Neo
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·Ilivia 7 VR-T DX, Intica 7 VR-T DX, Intica 5 VR-T DX, Ilivia 7 VR-T, Ilivia 7 DF4 VR-T, Intica 7 VR-T, Intica 7 DF4 VR-T
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Ilivia Neo 7 VR-T DX, Ilivia Neo 7 VR-T, Intica Neo 7 VR-T, Intica Neo 5 VR-T DX, Intica Neo 5 VR-T
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·LUMAX FAMILY OF ICDS AND CRT-DS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·Rayner C-flex 570C, C-Flex Aspheric 970C and 600C Aspheric Intraocular lenses
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·COMBI 40+COCHLEAR IMPLANT SYSTEM,C40+S(COMPRESSED)ELECTRODE ARRAY/C40+ GB (SPLIT) ELECTRODE ARRAY
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM WITH C40+, C40+S, OR C40+GB IMPLANTS, AND CIS PRO+/TEMPO+ SPEECH PROCESSORS
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·COMBI 40+ COCHLEAR IMPLANT SYSTEM
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM WITH C40+, C40+S, OR C40+GB IMPLANTS, AND CIS PRP+/TEMPO+ SPEECH PROCESSORS
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM; MED-EL COMBI 40+ (STANDARD), COMBI 40+S (COMPRESSED), AND COMBI 40+ GB (SPLITS
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·IGOTIS 5 HF-T (DF-4), 7 HF-T (DF-4, LI); IFORIA 7 HF-T (DF4, GB) IIESTO 5 HF-TIESTO 5 HF-T (DF-4)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·Perclose ProGlide Suture-Mediated Closure System, Perclose ProStyle Suture-Mediated Closure and Repair System