10,000 results · 45ms · Sources: EU EUDAMED, US FDA

FlexPasser Tendon Retrieval Kit

FDA registration
Systagenix Wound Management Manufacturing Limited·1 product·🇬🇧 United Kingdom

Systagenix Wound Management Manufacturing Limited

FDA registration
Systagenix Wound Management Manufacturing Limited·1 product·🇬🇧 United Kingdom

Systagenix Wound Management Manufacturing Limited

FDA registration
Systagenix Wound Management Manufacturing Limited·1 product·🇬🇧 United Kingdom

Systagenix Wound Management Manufacturing Limited

FDA registration
Systagenix Wound Management Manufacturing Limited·1 product·🇬🇧 United Kingdom

CC-Hook

FDA registration
Systagenix Wound Management Manufacturing Limited·1 product·🇬🇧 United Kingdom

XXL ARX Patella Tendon Long

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

XS ARX Patella Tendon Long

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

XL ARX Patella Tendon Long

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

S ARX Patella Tendon Long

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

M ARX Patella Tendon Long

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

L ARX Patella Tendon Long

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

XXXL ARX Patella Tendon Long

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

XXL ARX Basic Open Patella

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

XXXL ARX Basic Open Patella

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

XS ARX Basic Open Patella

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

XL ARX Basic Open Patella

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

S ARX Basic Open Patella

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

M ARX Basic Open Patella

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

L ARX Basic Open Patella

Device
EU MDR · Eu Md Class 1 ·Mediroyal Nordic AB·On the market

Intracranial Coil-Assist Stent

FDA Pre-Market Approval
FDA Class 3 ·Low-Profile Visualized Intraluminal Support (LVIS) and LVIS Jr.