17 results
·
43ms
·
Sources: EU EUDAMED, US FDA
Intervertebral fusion device
FDA registration
B & G MFG. CO.·2 products·🇺🇸 United States
ANTHEM
FDA registration
GLOBUS MEDICAL, INC.·2 products·🇺🇸 United States
Hipp Medical AG
FDA registration
Hipp Medical AG·2 products·🇩🇪 Germany
SMB MEDICAL SA
FDA registration
SMB MEDICAL SA·1 product·🇨🇭 Switzerland
ANTHEM Fracture System
FDA 510(k)
FDA Class 2
·Orthopedic
Ophthalmic Knife
FDA UDI
KATENA PRODUCTS, INC.·00841668113431·CRESCENT KNIFE DOUBLE BEVEL (BX/5)
Blade Scalpel
FDA UDI
KATENA PRODUCTS, INC.·00841668113516·MINIATURE BLADE #69 (BX/5)
Blade Scalpel
FDA UDI
KATENA PRODUCTS, INC.·00841668113493·LAMELLAR BLADE #66-60 (BX/5)
FriCARE Medical (Dongguan) Co., Ltd
FDA registration
FriCARE Medical (Dongguan) Co., Ltd·1 product·🇨🇳 China
N Latex FLC lambda
FDA registration
Siemens Healthcare Diagnostics Products GmbH·2 products·🇩🇪 Germany
ECOGUARD INC
FDA registration
ECOGUARD INC·1 product·🇺🇸 United States
M5 Recorder
FDA registration
Emsere, Inc.·2 products·🇺🇸 United States
MODEL 4815 ADAPTER
FDA 510(k)
FDA Class 2
·Cardiovascular
POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS
FDA 510(k)
FDA Class 3
·Cardiovascular
Plate, Fixation, Bone
FDA classification
FDA Class 2
·Plate, Fixation, Bone
Reservoir, Blood, Cardiopulmonary Bypass
FDA classification
FDA Class 2
·Reservoir, Blood, Cardiopulmonary Bypass
Automated External Defibrillators (Non-Wearable)
FDA classification
FDA Class 3
·Automated External Defibrillators (Non-Wearable)