5,404 results · 41ms · Sources: EU EUDAMED, US FDA

MAC 3500

FDA registration
GE Medical Systems Information Technologies - Critikon de Mexico S. de R.L. de C.V.·3 products·🇲🇽 Mexico

Cable

FDA registration
Amphenol Medical Technologies (Dongguan) Co., Ltd.·3 products·🇨🇳 China

MAC 5500 HD, MAC 3500

FDA registration
Cardiabase·3 products·🇫🇷 France

AltaTrack Guidewire

FDA registration
Volcano Corporation·3 products·🇺🇸 United States

MAC 2000 ECG ANALYSIS SYSTEM

FDA registration
Cardiabase·3 products·🇫🇷 France

QUANTIEN™ Measurement System with Software Version 1.12.1

FDA registration
St. Jude Medical, Cardiology Division, Inc.·3 products·🇺🇸 United States

Optis Mobile Next Imaging System

FDA registration
Abbott Medical·3 products·🇺🇸 United States

MAC 3500

FDA registration
GE Medical Systems Information Technologies, Inc.·3 products·🇺🇸 United States

IntelliVue Guardian Software Rev. C.1

FDA registration
Philips Medizin Systeme Boeblingen GmbH·3 products·🇩🇪 Germany

HemoSphere Advanced Monitor

FDA registration
BECTON, DICKINSON AND COMPANY·3 products·🇺🇸 United States

CSCS v2

FDA registration
WIPRO GE HEALTHCARE PRIVATE Ltd.·3 products·🇮🇳 India

MAC 7 - Resting ECG Analysis System

FDA registration
GE Medical Systems Information Technologies - Critikon de Mexico S. de R.L. de C.V.·3 products·🇲🇽 Mexico

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·ACRYSOF IQ TORIC INTRAOCULAR LENS (IOL)

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·AcrySof IQ Aspheric IOL with UltraSert

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·ACRYSOF(R) IQ TORIC INTRAOCULAR LENS

Lens, Multifocal Intraocular

FDA Pre-Market Approval
FDA Class 3 ·ACRYSOF IQ RESTOR IOLS +3.0 D

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval
FDA Class 3 ·Senza Spinal Cord Stimulation (SCS) System, Senza HFX iQ System

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·ACRYSOF IQ TORIC IOL WITH THE ULTRASERT PRE LOADED DELIVERY SYSTEM MODELS

Lens, Multifocal Intraocular

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

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·AcrySof Posterior Chamber Single Piece Intraocular Lenses