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