9 results
·
44ms
·
Sources: EU EUDAMED, US FDA
HA2 MEDIZINTECHNIK GMBH
FDA registration
HA2 MEDIZINTECHNIK GMBH·1 product·🇩🇪 Germany
HUMAN MED AG
FDA registration
HUMAN MED AG·1 product·🇩🇪 Germany
Puregraft 850
FDA registration
Bimini Health Tech·1 product·🇺🇸 United States
GID 700; Revolve; The Revolve System
FDA registration
LIFECELL CORP.·1 product·🇺🇸 United States
Harmac2308 (WP) - Puregraft 850 System
FDA registration
Synergy Health Westport Ltd·1 product·🇮🇪 Ireland
HARMAC MEDICAL PRODUCTS
FDA registration
HARMAC MEDICAL PRODUCTS·1 product·🇮🇪 Ireland
GID 700; Revolve; The Revolve System
FDA registration
LIFECELL CORP·1 product·🇺🇸 United States
LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension
FDA 510(k)
FDA Class 2
·Cardiovascular
Catheter, Percutaneous
FDA classification
FDA Class 2
·Catheter, Percutaneous