10,000 results · 49ms · Sources: EU EUDAMED, US FDA

BluPRO®

FDA UDI
NIHON KOHDEN CORPORATION·14931921878597·SpO2 probe Child / Infant (from 3 to 20 kg) Fin...

BluPRO®

FDA UDI
NIHON KOHDEN CORPORATION·04931921005828·SpO2 probe Adults (30 kg or more) Finger or toe...

Finapres

FDA UDI
Finapres Medical Systems B.V.·08719327007105·Finapres NOVA Main Unit NC

Finapres

FDA UDI
Finapres Medical Systems B.V.·08719327003770·Finger cuff size Large NC

NA

FDA UDI
NIHON KOHDEN CORPORATION·04931921854242·Electrode lead, 3 electrodes (AHA) (Snap type),

Vios Montioring System Adapter

FDA UDI
MURATA VIOS, INC.·B595L2050G0·The Vios Monitoring System (VMS) Adapter and Ch...

BluPRO®

FDA UDI
NIHON KOHDEN CORPORATION·14931921878535·SpO2 probe Adults (30 kg or more) Finger or toe...

BluPRO®

FDA UDI
NIHON KOHDEN CORPORATION·14931921878573·SpO2 probe Adults (40 kg or more) Finger or toe...

Vios Monitoring System Bedside Monitor

FDA UDI
MURATA VIOS, INC.·B595BSM20500·The Vios Monitoring System (VMS) Bedside Monito...

BluPRO®

FDA UDI
NIHON KOHDEN AMERICA, INC.·10841983102742·SpO2 probe Child / Infant (from 3 to 20 kg) Fin...

Vios Monitoring System Chest Sensor

FDA UDI
MURATA VIOS, INC.·B595CS20500·The Vios Monitoring System (VMS) Adapter and Ch...

BluPRO®

FDA UDI
NIHON KOHDEN CORPORATION·14931921878559·SpO2 probe Child (from 10 to 50 kg) Finger or t...

NA

FDA UDI
NIHON KOHDEN AMERICA, INC.·00841983100178·Electrode lead, 3 electrodes (AHA) (Snap type),

BluPRO®

FDA UDI
NIHON KOHDEN AMERICA, INC.·10841983102735·SpO2 probe Adults (40 kg or more) Finger or toe...

Defibrillator, Implantable, Dual-Chamber

FDA Pre-Market Approval
FDA Class 3 ·IFORIA/ILESTO/INVENTRA/IPERIA/ITREVIA 5/7 DR-T/VR-T/VR-T DX, & VARIOUS LUMAX ICDS; IFORIA/ILESTO/IPERIA/ITREVIA 5/7 HF-T

Defibrillator, Implantable, Dual-Chamber

FDA Pre-Market Approval
FDA Class 3 ·LUMAX 300/340/500/540 DR/DR-T/VR/VR-T/LUMAX 540 VR-T DX/KRONOS LV-T/LUMAX 300/340/500/540 HF/HF-T

Defibrillator, Implantable, Dual-Chamber

FDA Pre-Market Approval
FDA Class 3 ·LUMAX 300/340/500/540 DR/DR-T/VR/VR-T/LUMAX 540 VR-T DX/KRONOS LV-T/LUMAX 300/340/500/540 HF/HF-T

Pacemaker/Icd/Crt Non-Implanted Components

FDA Pre-Market Approval
FDA Class 3 ·ACTROS/AXIOS DR/SR/SLR/D/S, BA03 DDDR, CYLOS DR/DR-T/VR, DROMOS DR/SR/SL, KAIROS DR/SR/SL/D/S, PHILOS DR/D

CardioView

FDA registration
MEDEIA INC·6 products·🇺🇸 United States

ViSi Mobile Monitoring System

FDA registration
SOTERA WIRELESS·6 products·🇺🇸 United States