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)