21 results · 41ms · Sources: EU EUDAMED, US FDA

86547 5.5 Uncuffed Reinforced Tracheal Tube Murphy

FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States

Uncuffed Reinforced Trach. Tube

FDA registration
Covidien·1 product·🇺🇸 United States

Uncuffed Reinforced Trach. Tube

FDA registration
Covidien·1 product·🇲🇽 Mexico

Shiley Tracheal Tube Cuffless Reinforced

FDA registration
MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

UNCUFFED REINFORCED TRACHEAL TUBE

FDA 510(k)
FDA Class 2 ·Anesthesiology

PROLENE on TEFLON Pledget Buttress

FDA registration
ETHICON, LLC·1 product·🇺🇸 United States

PROLENE on TEFLON Pledget Suture Buttress

FDA registration
ETHICON, INC.·1 product·🇲🇽 Mexico

Patch, Pledget and Intracardiac, PETP, PTFE, Polypropylene - DeRoyal

FDA registration
DeRoyal Industries, Inc.·1 product·🇺🇸 United States

Patch, Pledget and Intracardiac, PETP, PTFE, Polypropylene - DeRoyal

FDA registration
DeRoyal Industries, Inc.·1 product·🇺🇸 United States

Patch, Pledget and Intracardiac, PETP, PTFE, Polypropylene - DeRoyal

FDA registration
DEROYAL INDUSTRIES, INC.·1 product·🇺🇸 United States

PROLENE on TEFLON Pledget Suture Buttress

FDA registration
ETHICON, INC.·1 product·🇺🇸 United States

CREATININE REAGENT

FDA registration
CLINIQA CORPORATION·1 product·🇺🇸 United States

Patch, Pledget and Intracardiac, PETP, PTFE, Polypropylene - DeRoyal

FDA registration
DEROYAL INDUSTRIES, INC.·1 product·🇺🇸 United States

PROLENE on TEFLON Pledget Suture Buttress

FDA registration
ETHICON, INC.·1 product·🇺🇸 United States

Patch, Pledget and Intracardiac, PETP, PTFE, Polypropylene - DeRoyal

FDA registration
DEROYAL INDUSTRIES, INC.·1 product·🇺🇸 United States

Tube, Tracheal (W/Wo Connector)

FDA classification
FDA Class 2 ·Tube, Tracheal (W/Wo Connector)

Sterigenics U.S., LLC

FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States

SUDOSCAN

FDA 510(k)
FDA Class 2 ·Neurology

ASCENT POROUS OPEN BOX PS COMPONENT/ASCENT POSTERIOR STABALIZED (PS) DISTAL FEMORAL PEGS

FDA 510(k)
FDA Class 2 ·Orthopedic

Device, Galvanic Skin Response Measurement

FDA classification
FDA Class 2 ·Device, Galvanic Skin Response Measurement