FDA Pre-Market Approval

INSYNC SENTRY/III MARQUIS/II MARQUIS/MAXIMO/CONCERTO ICDS/CONSULTA/MAXIMO II/CONCERTO II CRT-DS

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA Pre-Market Approval

FDA Class 3 ·PROMOTE, PROMOTE QUADRA, UNIFY, UNIFY QUADRA, UNIFY ASSURA AND QUADRA ASSURA FAMILIES OF CRT-D DEVICES

FDA Pre-Market Approval

MEDTRONIC PROTECTA XT/PROTECTA/CONSULTA/MAXIMO II CRT-D DF4 DEVICES (D314TRM, D334TRM, D204TRM AND D264TRM)

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval

FDA Class 3 ·Accolade Cardiac Resynchronization Therapy-Pacemaker (CRT-P) Devices: INVIVE TM, INTUA TM, VALITUDE, VALITUDE X4, VISION

Defibrillator, Implantable, Dual-Chamber

FDA Pre-Market Approval

FDA Class 3 ·Tupos LV/ATX & Kronos LV-T CRT-D and Corox OWT Steroid LV Pacing Lead

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Plexa ProMRI DF- S DX 65/15/17; IIivia 7 DR-T; Inrica 5 DTR-T

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA Pre-Market Approval

FDA Class 3 ·PROMOTE+, PROMOTE ACCEL, PROMOTE QUADRA, UNIFY, UNIFY QUADRA, QUADRA ASSURA FAMI LIES OF CRT-D DEVICES

Defibrillator, Implantable, Dual-Chamber

FDA Pre-Market Approval

FDA Class 3 ·Tupos LV/ATX & Kronos LV-T CRT-D & Corox OWT Steroid LV Pacing Lead

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA Pre-Market Approval

FDA Class 3 ·Cardiac Resynchronization Therapy Defibrillator (CRT-D) - Origne: G050, G051, G056, G058 - Inogen: G140, G141, G146, G14

BluPRO®

FDA UDI

NIHON KOHDEN AMERICA, INC.·00841983102691·Multi-site probe Adults, child (3 kg or more)

BluPRO®

FDA UDI

NIHON KOHDEN CORPORATION·04931921871188·Multi-site probe Adults, child (3 kg or more)

BluPRO®

FDA UDI

NIHON KOHDEN AMERICA, INC.·04931921019696·Multi-site probe Adults, child (3 kg or more)

BluPRO®

FDA UDI

NIHON KOHDEN AMERICA, INC.·00841983102684·Finger probe Adult, child (20kg or more) Finger

BluPRO®

FDA UDI

NIHON KOHDEN CORPORATION·04931921852712·Finger probe Adult, child (20kg or more) Finger

NA

FDA UDI

NIHON KOHDEN AMERICA, INC.·10841983102674·SpO2 probe Child, infant (from 3 to 15 kg) Toe,...

NA

FDA UDI

NIHON KOHDEN CORPORATION·14931921829445·SpO2 probe Child, infant (from 3 to 15 kg) Toe,...

NRT - Nordisk Røntgen Teknik A/S

System producer

🇩🇰 Denmark

KRIO Intézet Sejt- és Szövetbank Zrt.

System producer

🇭🇺 Hungary

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA Pre-Market Approval

FDA Class 3 ·Amplia, Amplia Brava ,Brava Quad, Claria Claria Quard, Compia, Consulta, Protecta, Viva MRI XT S CRT-D

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval

FDA Class 3 ·Allure, Allure RF, Allure Quadra, Allure Quadra RF, Quadra Allure, Quadra Allure MP family of CRT-Ps