21 results · 45ms · Sources: EU EUDAMED, US FDA

GLOBAL PROTECTION CORP.

FDA registration
GLOBAL PROTECTION CORP.·1 product·🇺🇸 United States

INNOLATEX (THAILAND) LIMITED

FDA registration
INNOLATEX (THAILAND) LIMITED·1 product·🇹🇭 Thailand

KAREX INDUSTRIES SDN BHD

FDA registration
KAREX INDUSTRIES SDN BHD·1 product·🇲🇾 Malaysia

ONE Nitrile Condom

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

Condom, Synthetic

FDA classification
FDA Class 2 ·Condom, Synthetic

DePuy Synthes MatrixSTERNUM Fixation System

FDA registration
SYNTHES GMBH·2 products·🇨🇭 Switzerland

DePuy Synthes MatrixSTERNUM Fixation System

FDA registration
DePuy Synthes Sales·2 products·🇺🇸 United States

DePuy Synthes MatrixSTERNUM Fixation System

FDA registration
Jabil Inc. (Monument)·2 products·🇺🇸 United States

Sensititre 20-24 hour H. influenzae/Strep.. pneumoniae(HP)MIC or BP Susceptibility System with ceftriaxone 015 - 2 ug/

FDA registration
TREK DIAGNOSTIC SYSTEMS, LTD.·3 products·🇬🇧 United Kingdom

DePuy Synthes MatrixSTERNUM Fixation System

FDA registration
Jabil Switzerland Manufacturing GmbH (Hagendorf)·2 products·🇨🇭 Switzerland

DePuy Synthes MatrixSTERNUM Fixation System

FDA registration
Synthes (USA) Products LLC·2 products·🇺🇸 United States

DePuy Synthes MatrixSTERNUM Fixation System

FDA registration
Synthes GMBH·2 products·🇨🇭 Switzerland

DePuy Synthes MatrixSTERNUM Fixation System

FDA registration
Jabil Inc. (Brandywine)·2 products·🇺🇸 United States

DePuy Synthes MatrixSTERNUM Fixation System

FDA registration
Avalign Delivery Systems Division·2 products·🇺🇸 United States

DePuy Synthes MatrixSTERNUM Fixation System

FDA registration
Jabil Switzerland Manufacturing GmbH (Grenchen)·2 products·🇨🇭 Switzerland

DePuy Synthes MatrixSTERNUM Fixation System

FDA registration
DEPUY ORTHOPAEDICS·2 products·🇺🇸 United States

Loss of Pulse Detection

FDA registration
FITBIT LLC·1 product·🇺🇸 United States

ValvuloPro Valvuloplasty Balloon Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

DePuy Synthes MatrixSTERNUM Fixation System

FDA 510(k)
FDA Class 2 ·Orthopedic

Balloon Aortic Valvuloplasty

FDA classification
FDA Class 2 ·Balloon Aortic Valvuloplasty