10,000 results
·
54ms
·
Sources: EU EUDAMED, US FDA
TRICON
FDA registration
Smith & Nephew, Inc.·1 product·🇺🇸 United States
TRICON
FDA registration
Smith & Nephew, Inc.·1 product·🇺🇸 United States
Zimmer Biomet Pty Ltd
FDA registration
Zimmer Biomet Pty Ltd·1 product·🇦🇺 Australia
TRICON
FDA registration
Smith & Nephew, Inc.·1 product·🇺🇸 United States
ZIMMER PTE. LTD.
FDA registration
ZIMMER PTE. LTD.·1 product·🇸🇬 Singapore
OFFSET TIBIAL TRAY
FDA registration
BIOMET, INC.·1 product·🇺🇸 United States
Zimmer (LN) - OFFSET TIBIAL TRAY
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
TRICON
FDA registration
Smith & Nephew, Inc.·1 product·🇺🇸 United States
OFFSET TIBIAL TRAY
FDA registration
Changzhou Biomet Medical Devices Co., Ltd.·1 product·🇨🇳 China
Smith and Nephew
FDA registration
ARVATO USA LLC·1 product·🇺🇸 United States
TRICON
FDA registration
SMITH & NEPHEW, INC.·1 product·🇺🇸 United States
Zimmer (Shanghai) Medical International Trading Co., Ltd.
FDA registration
Zimmer (Shanghai) Medical International Trading Co., Ltd.·1 product·🇨🇳 China
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Emblem S-ICD Programmer - Plexus SMT Mfg. Line
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509
LIPASE DETERMINATION
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SERUM LIPASE REAGENT SET (TURBIDIMETRIC)
FDA 510(k)
FDA Class 1
·Clinical Chemistry
TRUCATH.IP
FDA 510(k)
FDA Class 2
·Immunology