153 results
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73ms
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Sources: EU EUDAMED, US FDA
Sanitas™ Clinical Care Platform
FDA UDI
SANITAS, INC.·00860508000311·The Sanitas™ Clinical Care Platform is a softwa...
Family Healthware™
FDA UDI
SANITAS, INC.·00860508000304·Family Healthware™ is a self-administered, inte...
WELLAHO PERSONALIZED OUTPATIENT MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
FAMILY HEALTHWARE
FDA 510(k)
FDA Class 2
·Cardiovascular
HEMO-SANITAS SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
Acecide-C
FDA registration
Best Sanitizers, Inc.·1 product·🇺🇸 United States
FDA Pre-Market Approval
COHERENT PDL1 AND PDL2 LAMBDA PLUS PHOTODYNAMIC LASERS
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·EZ STEER THERMOCOOL CATHETERS
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·ANEURX STENT GRAFT SYSTEM
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·NAVISTAR THERMOCOOL
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·NAVISTAR DS/NAVISTAR RMT DS/EZ STEER NAV DS/QWIKSTAR DS
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CELSIUS THERMOCOOL & NAVISTAR THERMOCOOL
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CELSIUS CATHETER, NON-TEMPERATURE SENSING ABLATION CATHETERS, INTERFACE CABLES
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·NAVISTAR CATHETER, INTERFACE CABLES
Transcervical Contraceptive Tubal Occlusion Device
FDA Pre-Market Approval
FDA Class 3
·ESSURE CONTRACEPTIVE TUBAL OCCLUSION DEVICE AND DELIVERY SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASCULAR CLOSURE SYSTEMS
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·SUTURE MEDIATED CLOSURE SYSTEMS & ASSOCIATED ACCESSORIES
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·GORE EXCLUDER AAA ENDOPROSTHESIS, GORE EXCLUDER ILIAC BRANCH ENDOPROSTHESIS
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Senza Spinal Cord Stimulation (SCS) System
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·PROLIEVE THERMODILATATION SYSTEM CATHETER AND HEAT EXCHANGER