DIGI-PRO TENS, MODEL WL-2204 AND WL-2205

FDA 510(k)

FDA Class 2 ·Physical Medicine

DIGI-PRO TENS/WL-2203B,2204B,2204B-P1,2204B-P2,2205B

FDA 510(k)

FDA Class 2 ·Neurology

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC ARRHYTHMIA MANAGEMENT DEVICES INCLUDING MODEL 7221B/CX/D/E MICRO JEWEL DEVICE USED WITH CPI ENDOTAK

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC ARRHYTHMIA MANAGEMENT DEVICES INCLUDING MODEL 7221B/CX/D/E MICRO JEWEL DEVICE USED WITH CPI ENDOTAK

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC ARRHYTHMIA MANAGEMENT DEVICES INCLUDING MODEL 7221B/CX/D/E MICRO JEWEL DEVICE USED WITH CPI ENDOTAK

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC ARRHYTHMIA MANAGEMENT DEVICES INCLUDING MODEL 7221B/CX/D/E MICRO JEWEL DEVICE USED WITH CPI ENDOTAK

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC ARRHYTHMIA MANAGEMENT DEVICES INCLUDING MODEL 7221B/CX/D/E MICRO JEWEL DEVICE USED WITH CPI ENDOTAK

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC ARRHYTHMIA MANAGEMENT DEVICES INCLUDING MODEL 7221B/CX/D/E MICRO JEWEL DEVICE USED WITH CPI ENDOTAK

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC ARRHYTHMIA MANAGEMENT DEVICES INCLUDING MODEL 7221B/CX/D/E MICRO JEWEL DEVICE USED WITH CPI ENDOTAK

Cursus3

Basic UDI-DI

EU MDR · Eu Md Class 1 ·GPI France·1 device

EMOLIFE

Basic UDI-DI

EU MDR · Eu Md Class 2b ·GPI S.P.A.·1 device

TENGEER

Basic UDI-DI

EU MDR · Eu Md Class 2a ·GPI S.P.A.·1 device

PHEBO

Basic UDI-DI

EU MDR · Eu Md Class 2a ·GPI S.P.A.·1 device

OLV VISICAT + TRAY

Basic UDI-DI

EU MDR · Eu Md Class 1 ·Ippi srl·10 devices

AsTer Total Care

Basic UDI-DI

EU MDR · Eu Md Class 2a ·GPI S.P.A.·1 device

EMONET

Basic UDI-DI

EU MDR · Eu Md Class 2b ·GPI S.P.A.·1 device

NGH MD

Basic UDI-DI

EU MDR · Eu Md Class 2b ·GPI S.P.A.·1 device

Hematos IIG

Basic UDI-DI

EU MDR · Eu Md Class 1 ·GPI France·1 device

POHEMA (versione 2)

Basic UDI-DI

EU MDR · Eu Md Class 2a ·GPI S.P.A.·1 device

System, Laser, Photodynamic Therapy

FDA Pre-Market Approval

FDA Class 3 ·PHOTOFRIN 630 PDT Laser