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DF1-1069 B BARRES PARALLELES FIXES 5M

Basic UDI-DI
EU MDD · Eu Md Class 1 ·ETABLISSEMENTS FRANCO ET FILS·1 device

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Lead Cap (IS-1/DF-1/SJ4/DF/IS4) IS4/DF4 Port Plug; DF-1 Receptacle Plug; IS-1 Receptacle Plug

Disc-FX® Guidewire

FDA UDI
ELLIQUENCE, LLC·00846338010911·

Disc-FX® Guidewire

FDA UDI
ELLIQUENCE, LLC·00846338001476·

Disc-FX® Guidewire

FDA UDI
ELLIQUENCE, LLC·00846338001483·

DIAGNOSTIC ULTRASOUND SYSTEM, TYPE 3535, MODIFIED

FDA 510(k)
FDA Class 2 ·Radiology

DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535, MODIFIED

FDA 510(k)
FDA Class 2 ·Radiology

ULTRASOUND SCANNER 2002

FDA 510(k)
FDA Class 2 ·Radiology

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Protego SD; Protego TD; Protego DF-1 SD; Protego ProMRI SDx; Protego DF-1; ProMRI SD; Plexa SD; Plexa ProMRI SD; Plexa D

DPK Kft.

Importer
🇭🇺 Hungary

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

FDA Pre-Market Approval
FDA Class 3 ·Iperia 7 HF-T (DF-1) Iperia 7 HF-T (DF4) Inventra 7 HF-T (DF-1) Inventra 7 HF-T (DF4) Defibrillator, Automatic Implantab

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Cobalt MRI ICD, Cobalt MRI ICD, Cobalt XT MRI, Cobalt XT MRI, Crome MRI ICD, Crome MRI ICD,Evera MRI DF-1,Evera MRI DF-1

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Cobalt MRI ICD; Cobalt MRI ICD; Cobalt XT MRI ICD; Crome MRI ICD; Evera MRI DF-1 ICD; Evera MRI DF-1 ICD; Evera MRI ICD;

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Evera MRI DF-1 ICD / Evera S DR /VR ICD / Evera XT VR ICD / Protecta ICD / Protecta XT ICD /Visia AF MRI DF 1 ICD / Visi

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Evera MRI DF-1, Evera MRI ICD's; Mirro MIR DR, Mirro MIR VR ICD's; Primo MRI DR, Primo MRI VR ICD's; Visia AF MRI DF1, V

Stretcher

Basic UDI-DI
EU MDR · Eu Md Class 1 ·Shanghai DNK New Materials Technology Co., Ltd.·1 device

Carbon fiber electric wheelchair

Basic UDI-DI
EU MDR · Eu Md Class 1 ·Shanghai DNK New Materials Technology Co., Ltd.·1 device

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·ACRYSOF RESTOR INTRAOCULAR LENS

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·AcrySof IQ ReSTOR Posterior Chamber Intraocular Lenses

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·AcrySof IQ ReSTOR Posterior Chamber Intraocular Lenses