9,794 results
·
47ms
·
Sources: EU EUDAMED, US FDA
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·INVIVE, INTUA, VISIONIST and VALITUDE (CRT-P Resynchronization Devices)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·INGENIO MRI, VITALIO MRI, FORMIO MRI, ESSENTIO MRI, PROPONENT MRI and ACCOLADE MRI (Pacemaker Devices)
Impla-NX (Model: ISE-270M)
FDA 510(k)
FDA Class 1
·Dental
Dental Handpiece, Model CA160, CA160L, and CA500L
FDA 510(k)
FDA Class 1
·Dental
NX STAGE WATER PURIFICATION SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MEG-TORQ
FDA 510(k)
FDA Class 1
·Dental
Dental Handpiece, Wireless Endodontic Handpiece, endoit
FDA 510(k)
FDA Class 1
·Dental
ELEC-LED
FDA 510(k)
FDA Class 1
·Dental
Dental Handpiece
FDA 510(k)
FDA Class 1
·Dental
0417,APS, N,CH,LT & LED'S',SF
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828152600·0417,APS, N,CH,LT & LED'S',SF
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·LATITUDE NXT 2.0 PATIENT MANAGEMENT SYSTEM
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·LATITUDE NXT Release Patient Management System
NA
FDA UDI
PROTEUS DIGITAL HEALTH, INC.·10856602005045·
Pathfinder
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522125645·PATHFINDER SL/SENTINEL 10 EVAL SYSTEM (ENG)
Proteus Digital Health Feedback System
FDA UDI
PROTEUS DIGITAL HEALTH, INC.·00856602005222·
NA
FDA UDI
PROTEUS DIGITAL HEALTH, INC.·10856602005243·
Sentinel
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522123238·SENTINEL 10.0.1 ADD. NETWORK WORKSTAT LICENSE EN
NA
FDA UDI
PROTEUS DIGITAL HEALTH, INC.·10856602005182·
Proteus Digital Health Feedback System
FDA UDI
PROTEUS DIGITAL HEALTH, INC.·00856602005130·
Sentinel
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522103100·SENTINEL 10 WORKSTATION (X2) + ABP LICENSE