Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MODEL 2490G/H/J MEDTRONIC CARELINK MONITOR AND THE MODEL 2020A CARDIOSIGHT READER

HX-3 Horizontal Fold Flat FFP3

Basic UDI-DI

EU MDR · Eu Md Class 1 ·Alpha Solway Ltd·1 device

HX-2 Horizontal Fold Flat FFP2

Basic UDI-DI

EU MDR · Eu Md Class 1 ·Alpha Solway Ltd·1 device

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR SYSTEMS

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC PACEMAKER SYSTEMS

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR SYSTEMS

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC PACEMAKER SYSTEMS

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

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC CARDIAC RESYNCHRONIZATION THERAPY-DEFIBRILLATOR SYSTEMS

nSpire Health

FDA UDI

NSPIRE HEALTH, INC.·10852417003627·KoKo Standard Blue Filter Kit with Nose Clip an...

Vital Sync

FDA UDI

Covidien LP·10884521795143·Ventilation Dashboard v1.0 Subscription

Vital Sync

FDA UDI

Covidien LP·10884521795150·Ventilation Dashboard v1.0 Excess Use Subscription

nSpire Health

FDA UDI

NSPIRE HEALTH, INC.·10852417003719·KoKo Standard White Filter Kit with Nose Clip a...

nSpire Health

FDA UDI

NSPIRE HEALTH, INC.·10852417003757·KoKo Standard White Filter Kit with Nose Clip a...

nSpire Health

FDA UDI

NSPIRE HEALTH, INC.·10852417003696·KoKo Standard White Filter Kit with Nose Clip a...

CARESCAPE Central Station

FDA UDI

GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.·00840682109666·

nSpire Health

FDA UDI

NSPIRE HEALTH, INC.·10852417003665·KoKo Standard White Filter Kit with Nose Clip a...

CARESCAPE Central Station

FDA UDI

GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.·00840682109604·

Device, Incontinence, Urosheath Type, Non-Sterile

FDA classification

FDA Class 1 ·Device, Incontinence, Urosheath Type, Non-Sterile

Stimulator, Electrical, Implanted, For Parkinsonian Symptoms

FDA Pre-Market Approval

FDA Class 3 ·Vercise Genus DBS System, Vercise Gevia DBS System, Vercise PC DBS System

Vios Monitoring System

FDA registration

Murata Vios, Private Limited·7 products·🇮🇳 India