153 results · 73ms · 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