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