20 results
·
50ms
·
Sources: EU EUDAMED, US FDA
JW-120B
FDA registration
Nihon Kohden Tomioka Corporation·1 product·🇯🇵 Japan
JW-120B
FDA registration
NIHON KOHDEN AMERICA, INC.·1 product·🇺🇸 United States
JW-120B
FDA registration
Nihon Kohden Corporation - Tokorozawa establishment Advanced Technology Center·1 product·🇯🇵 Japan
JW-120B
FDA registration
NIHON KOHDEN TOMIOKA PRODUCTION CENTER·1 product·🇯🇵 Japan
JW-120B
FDA registration
NIHON KOHDEN CORP.·1 product·🇯🇵 Japan
JW-120B
FDA registration
Nihon Kohden Corporation - Eastern Japan Logistics Center·1 product·🇯🇵 Japan
SEN-4100 ELECTRIC STIMULATOR
FDA 510(k)
FDA Class 2
·Neurology
K071959
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
SYNTHES CERVIFIX SYSTEM; K011969
FDA registration
EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States
Stimulator, Electrical, Evoked Response
FDA classification
FDA Class 2
·Stimulator, Electrical, Evoked Response
Restore
FDA registration
DEPUY ORTHOPAEDICS, INC.·1 product·🇺🇸 United States
SYNTHES CERVIFIX SYSTEM
FDA registration
Synthes (USA) Products LLC·1 product·🇺🇸 United States
Jabil Inc. (Brandywine)
FDA registration
Jabil Inc. (Brandywine)·1 product·🇺🇸 United States
APPLIANCE, FIXATION, SPINAL INTERLAMINAL
FDA registration
SYNTHES GMBH·1 product·🇨🇭 Switzerland
Victory LX Sport (S710LXW)
FDA registration
Guangdong Marshell Electric Vehicle CO., LTD.·1 product·🇨🇳 China
AMPLATZER Vascular Plug - II ES
FDA registration
Abbott Vascular Netherlands·1 product·🇳🇱 Netherlands
SYNTHES CERVIFIX SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
GT2 FUSION GUIDE WIRE, MODEL NTLHLJ180,NTLHLS180, NTLHLJ300, NTLHLS300
FDA 510(k)
FDA Class 2
·Cardiovascular
Appliance, Fixation, Spinal Interlaminal
FDA classification
FDA Class 2
·Appliance, Fixation, Spinal Interlaminal
Catheter, Percutaneous
FDA classification
FDA Class 2
·Catheter, Percutaneous