9,715 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Response with Lumen
FDA registration
St. Jude Medical, Atrial Fibrillation Division, Inc.·1 product·🇺🇸 United States
St. Jude Medical
FDA registration
St. Jude Medical·1 product·🇺🇸 United States
REFSTAR PLUS with QWIKPATCH External REference Patch, REFSTAR PLUS Cable
FDA registration
BIOSENSE WEBSTER, INC.·1 product·🇺🇸 United States
CS Assist Diagnostic Catheter
FDA registration
C.R. BARD, INC.·1 product·🇺🇸 United States
TapCath
FDA registration
CARDIOCOMMAND, INC.·1 product·🇺🇸 United States
PARTER MEDICAL PRODUCTS, INC.
FDA registration
PARTER MEDICAL PRODUCTS, INC.·1 product·🇺🇸 United States
CORDIS WESTER STAR CATHETER
FDA registration
LARK INDUSTRIES·1 product·🇺🇸 United States
Inquiry
FDA registration
IRVINE BIOMEDICAL. INC.·1 product·🇺🇸 United States
LASSO NAV CATHETER
FDA registration
BIOSENSE WEBSTER, INC.·1 product·🇺🇸 United States
WovenFlexie Diagnostic Catheter
FDA registration
C.R. BARD, INC.·1 product·🇺🇸 United States
Boston Scientific Limited
FDA registration
Boston Scientific Limited·1 product·🇮🇪 Ireland
ViaCath
FDA registration
VASCOMED INST KATHETERTECHNOLOGIE·1 product·🇩🇪 Germany
Honeywell
FDA registration
Key Tronic Juarez, S.A de C.V.·1 product·🇲🇽 Mexico
Boston Scientific Corporation
FDA registration
Boston Scientific Corporation·1 product·🇺🇸 United States
MediGuide Enabled Livewire Steerable EP Catheter
FDA registration
St. Jude Medical, Atrial Fibrillation Division, Inc.·1 product·🇺🇸 United States
Biotronick, Inc.
FDA registration
Venusa de Mexico S. de R.L de C.V·1 product·🇲🇽 Mexico
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CONTAK RENEWAL 3 RF
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CONTAK RENEWAL 3 RF
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·RENEWAL 3 RF ICDS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·RENEWAL 3 RF FAMILIES